Triazolopyridine compound, and action thereof as prolyl hydroxylase inhibitor or erythropoietin production-inducing agent

ABSTRACT

The present invention provides a triazolopyridine compound having a prolyl hydroxylase inhibitory action and an erythropoietin production-inducing ability. The present invention relates to a compound represented by the following formula [I]: 
     
       
         
         
             
             
         
       
     
     wherein each symbol is as defined in the specification, or a pharmaceutically acceptable salt thereof, or a solvate thereof, as well as a prolyl hydroxylase inhibitor or erythropoietin production-inducing agent containing the compound. The compound of the present invention shows a prolyl hydroxylase inhibitory action and an erythropoietin production-inducing ability and is useful as a prophylactic or therapeutic agent for various diseases and pathologies (disorders) caused by decreased production of erythropoietin.

TECHNICAL FIELD

The present invention relates to a novel triazolopyridine compoundhaving a prolyl hydroxylase (hereinafter to be also referred to as“PHD”) inhibitory action and an erythropoietin (hereinafter alsoreferred to as “EPO”) production-inducing ability. The present inventionalso relates to a prolyl hydroxylase inhibitor (hereinafter to be alsoreferred to as “PHD inhibitor”) and an erythropoietinproduction-inducing agent (hereinafter to be also referred to as “EPOproduction-inducing agent”), each containing the triazolopyridinecompound.

BACKGROUND OF THE INVENTION

EPO is a hormone that promotes growth of red blood cell consisting of165 amino acids. EPO is mainly produced in the kidney and partly in theliver, and the production thereof increases under low oxygen conditions.

Anemia refers to a condition showing low levels of red blood cell andhemoglobin in the blood. The symptoms thereof are derived from oxygendeficiency due to decreased number of red blood cells, or changes of thecirculation dynamics due to increased breathing rate and cardiac rate tocompensate for the oxygen deficiency, and include “general sickfeeling”, “easily-fatigued”, “short breath”, “palpitation”, “heavinessof the head”, “dizziness”, “bad complexion”, “shoulder stiffness”,“difficulty in awakening in the morning” and the like.

The cause of anemia is largely divided into low production, promoteddestruction and promoted loss of red blood cells, and anemia includesanemia due to hematopoiesis abnormality in the bone marrow, anemia dueto shortage of iron, vitamin B₁₂ or folic acid, bleeding during accidentor operation, anemia associated with chronic inflammation (autoimmunediseases, malignant tumor, chronically-transmitted diseases, plasma celldyscrasia etc.), anemia associated with endocrine diseases(hypothyroidism, autoimmune polyglandular syndrome, type IA diabetes,dysfunctional uterine bleeding etc.), anemia associated with chroniccardiac failure, anemia associated with ulcer, anemia associated withhepatic diseases, senile anemia, drug-induced anemia, renal anemia(anemia associated with renal failure), anemia associated with chemicaltherapy, and the like.

In 1989, a gene recombinant human EPO preparation was approved by theU.S. Food and Drug Administration (FDA) for application to renal anemia,anemia associated with AZT treatment of HIV patients, anemia associatedwith chemical therapy of cancer patients, or for reduction of bloodtransfusion volume for patients who underwent an operation. Moreover,its application has been spreading to anemia of prematurity and thelike.

Renal anemia is treated with an erythropoiesis stimulating agent (ESA).Renal anemia is mainly caused by decreased EPO production in theinterstitial cells in the periphery of renal tubule of the kidney. It isan application wherein gene recombinant human erythropoietin is highlyoften used for supplement of EPO. Gene recombinant human erythropoietinhas strikingly reduced the number of patients in need of periodic bloodtransfusion, improved various symptoms associated with anemia andgreatly contributed to the improvement of ADL (Activities of dailyliving) and QOL (Quality of Life). On the other hand, being a biologicalpreparation, it is expensive and requires high medical expenses. Inaddition, it has a short half-life in blood and requires 2-3 times ofintravenous administration per week from the dialysis circuit inhemodialysis patients. Thus, the injection frequency is desired to bedecreased to prevent medical accidents, and also from the aspects of theamount of medical practice and waste. Furthermore, for peritonealdialysis patients and patients with renal failure in predialysis period,for whom subcutaneous administration affording a longer period ofduration has been employed, once per one or two weeks of administrationis still necessary. In this case, the patients often need to go to thehospital only for the administration of gene recombinant humanerythropoietin, causing burden on the patients.

Moreover, a long-acting EPO medicament having a prolonged half-life inblood by intravenous injection or subcutaneous injection has beendeveloped by modifying EPO by adding a new sugar chain or PEG chain.However, since only injection preparations have been developed, anorally administrable ESA is desired to prevent medical accidents andreduce burden on patients.

Moreover, an orally administrable ESA is expected to be applicable to awider range of treatments for not only renal anemia but also anemiacaused by various causes.

As a representative molecule promoting transcription of EPO, HypoxiaInducible Factor (hereinafter to be also referred to as “HIF”) can bementioned. HIF is a protein consisting of a heterodimer having an oxygenregulatory α-subunit and a constitutionally-expressed β-subunit, whereproline in the α-subunit is hydoxylated by prolyl hydroxylase (PHD) inthe presence of oxygen and the resulting α-subunit is bound to vonHippel-Lindau (VHL) protein and ubiquitinated. However, since α-subunitis not subject to hydroxylation by PHD under low oxygen conditions, itis not ubiquitinated but bound to an intranuclear hypoxia responseelement (HRE) to promote transcription of EPO present at the downstreamof HIF. Therefore, inhibition of the activity of PHD results in theprevention of ubiquitination of HIF and stabilization thereof.Consequently, the EPO production is increased.

Examples of the diseases expected to be improved by inhibiting PHD tostabilize HIF include ischemic cardiac diseases (angina pectoris,myocardial infarction etc.), ischemic cerebrovascular disorders(cerebral infarction, cerebral embolism, transient cerebral ischemicattack etc.), chronic renal failures (ischemic nephropathy, renal tubuleinterstitial disorder etc.), diabetic complications (diabetic woundetc.), cognitive impairments (dementia, Alzheimer's disease, Parkinson'sdisease, Huntington's disease etc.) and the like.

SUMMARY OF THE INVENTION Problems to be Solved by the Invention

From the findings obtained from the studies heretofore, it has beenclarified that a medicament inhibiting prolyl hydroxylase (PHD) promotesproduction of erythropoietin (EPO) and is effective for the prophylaxisor treatment of various diseases and pathologies (disorders) caused bydecreased production of EPO, particularly for the treatment of anemia.

Accordingly, the present invention aims to provide a medicament having aprolyl hydroxylase (PHD) inhibitory action. In addition, the presentinvention aims to provide a medicament having EPO production-inducingability.

Means of Solving the Problems

The present inventors have found a compound having a prolyl hydroxylase(PHD) inhibitory action and EPO production-inducing ability, andcompleted the present invention.

More particularly, the present invention provides the following.

[1] A compound represented by the following formula [I] (hereinafter tobe also referred to as “the compound of the present invention”) or apharmaceutically acceptable salt thereof, or a solvate thereof:

whereinthe partial structural formula:

is a group represented by any of the following formulas:

-   -   R¹ is        (1) a hydrogen atom,        (2) a C₁₋₆ alkyl group,        (3) a C₆₋₁₄ aryl group,        (4) a C₃₋₈ cycloalkyl group,        (5) a C₆₋₁₄ aryl-C₁₋₆ alkyl group, or        (6) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group;

R² is

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group,(3) a C₆₋₁₄ aryl group optionally substituted by the same or different 1to 5 substituents selected from the following group B,(4) a C₃₋₈ cycloalkyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from the following group B,(5) a C₃₋₈ cycloalkenyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from the following group B,(6) a heteroaryl group optionally substituted by the same or different 1to 5 substituents selected from the following group B (wherein theheteroaryl has, besides carbon atom, 1 to 6 hetero atoms selected fromnitrogen atom, oxygen atom and sulfur atom),(7) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe following group B), or(8) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group (wherein C₃₋₈ cycloalkyl isoptionally substituted by the same or different 1 to 5 substituentsselected from the following group B);

R³ is

(1) a hydrogen atom,(2) a halogen atom,(3) a C₁₋₆ alkyl group,(4) a C₆₋₁₄ aryl group,(5) a C₃₋₈ cycloalkyl group, or(6) a C₆₋₁₄ aryl-C₁₋₆ alkyl group; andR⁴ and R⁵ are each independently(1) a hydrogen atom, or(2) a C₁₋₆ alkyl group, group B:(a) a halogen atom,(b) a C₁₋₆ alkyl group,(c) a C₃₋₈ cycloalkyl group,(d) a cyano group, and(e) a halo-C₁₋₆ alkyl group.[2] The compound described in the above-mentioned [1] wherein thepartial structural formula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[3] The compound described in the above-mentioned [1], wherein thepartial structural formula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[4] The compound described in the above-mentioned [1], wherein thepartial structural formula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[5] The compound described in the above-mentioned [1], wherein thepartial structural formula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[6] The compound described in any of the above-mentioned [1] to [5],wherein both R⁴ and R⁵ are hydrogen atoms, or a pharmaceuticallyacceptable salt thereof, or a solvate thereof.[7] The compound described in any of the above-mentioned [1] to [5],wherein R³ is a hydrogen atom, or a pharmaceutically to acceptable saltthereof, or a solvate thereof.[8] The compound described in any of the above-mentioned [1] to [5],wherein R¹ is a hydrogen atom, or a pharmaceutically acceptable saltthereof, or a solvate thereof.[9] The compound described in any of the above-mentioned [1] to [5],wherein R² is(1) a C₁₋₁₀ alkyl group,(2) a C₆₋₁₄ aryl group optionally substituted by the same or different 1to 5 substituents selected from the above-mentioned group B,(3) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe above-mentioned group B), or(4) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group (wherein C₃₋₈ cycloalkyl isoptionally substituted by the same or different 1 to 5 substituentsselected from the above-mentioned group B), or a pharmaceuticallyacceptable salt thereof, or a solvate thereof.[10] The compound described in the above-mentioned [2], wherein both R⁴and R⁵ are hydrogen atoms, or a pharmaceutically acceptable saltthereof, or a solvate thereof.[11] The compound described in the above-mentioned [10], wherein R³ is ahydrogen atom, or a pharmaceutically acceptable salt thereof, or asolvate thereof.[12] The compound described in the above-mentioned [11], wherein R¹ is ahydrogen atom, or a pharmaceutically acceptable salt thereof, or asolvate thereof.[13] The compound described in the above-mentioned [12], wherein R² is(1) a C₁₋₁₀ alkyl group, or(2) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe above-mentioned group B),or a pharmaceutically acceptable salt thereof, or a solvate thereof.[14] A compound represented by the following formula [I-1] or apharmaceutically acceptable salt thereof, or a solvate thereof:

wherein the partial structural formula:

is a group represented by any of the following formulas:

R¹¹ is

(1) a hydrogen atom,(2) a C₁₋₆ alkyl group,(3) a phenyl group,(4) a C₃₋₈ cycloalkyl group,(5) a phenyl-C₁₋₆ alkyl group, or(6) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group;

R²¹ is

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group,(3) a phenyl group optionally substituted by the same or different 1 to5 substituents selected from the following group B,(4) a C₃₋₈ cycloalkyl group,(5) a C₃₋₈ cycloalkenyl group,(6) a thienyl group optionally substituted by the same or different 1 to5 substituents selected from the following group B,(7) a phenyl-C₁₋₆ alkyl group (wherein phenyl is optionally substitutedby the same or different 1 to 5 substituents selected from the followinggroup B), or(8) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group;

R³¹ is

(1) a hydrogen atom,(2) a halogen atom,(3) a C₁₋₆ alkyl group,(4) a phenyl group,(5) a C₃₋₈ cycloalkyl group, or(6) a phenyl-C₁₋₆ alkyl group; andR⁴¹ and R⁵¹ are each independently(1) a hydrogen atom, or(2) a C₁₋₆ alkyl group group B:(a) a halogen atom,(b) a C₁₋₆ alkyl group,(c) a C₃₋₈ cycloalkyl group,(d) a cyano group, and(e) a halo-C₁₋₆ alkyl group.[15] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[16] a compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[17] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[18] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[19] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[20] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[21] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[22] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[23] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[24] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[25] A compound represented by the following formula:

or a pharmaceutically acceptable salt thereof, or a solvate thereof.[26] A pharmaceutical composition comprising the compound described inany of the above-mentioned [1] to [25], or a pharmaceutically acceptablesalt thereof, or a solvate thereof, and a pharmaceutically acceptablecarrier (hereinafter to be also referred to as “the pharmaceuticalcomposition of the present invention”).[27] A prolyl hydroxylase inhibitor comprising the compound described inany of the above-mentioned [1] to [25], or a pharmaceutically acceptablesalt thereof, or a solvate thereof.[28] An erythropoietin production-inducing agent comprising the compounddescribed in any of the above-mentioned [1] to [25], or apharmaceutically acceptable salt thereof, or a solvate thereof.[29] A therapeutic agent for anemia comprising the compound described inany of the above-mentioned [1] to [25], or a pharmaceutically acceptablesalt thereof, or a solvate thereof.[30] A therapeutic agent for renal anemia comprising the compounddescribed in any of the above-mentioned [1] to [25], or apharmaceutically acceptable salt thereof, or a solvate thereof.[31] Use of the compound described in any of the above-mentioned [1] to[25], or a pharmaceutically acceptable salt thereof, or a solvatethereof, for the production of a prolyl hydroxylase inhibitor.[32] Use of the compound described in any of the above-mentioned [1] to[25], or a pharmaceutically acceptable salt thereof, or a solvatethereof, for the production of an erythropoietin production-inducingagent.[33] Use of the compound described in any of the above-mentioned [1] to[25], or a pharmaceutically acceptable salt thereof, or a solvatethereof, for the production of a therapeutic agent for anemia.[34] Use of the compound described in any of the above-mentioned [1] to[25], or a pharmaceutically acceptable salt thereof, or a solvatethereof, for the production of a therapeutic agent for renal anemia.[35] A method of inhibiting prolyl hydroxylase, comprising administeringan effective amount of the compound described in any of theabove-mentioned [1] to [25], or a pharmaceutically acceptable saltthereof, or a solvate thereof to a mammal.[36] A method of inducing erythropoietin production, comprisingadministering an effective amount of the compound described in any ofthe above-mentioned [1] to [25], or a pharmaceutically acceptable saltthereof, or a solvate thereof to a mammal.[37] A method of treating anemia, comprising administering an effectiveamount of the compound described in any of the above-mentioned [1] to[25], or a pharmaceutically acceptable salt thereof, or a solvatethereof to a mammal.[38] A method of treating renal anemia, comprising administering aneffective amount of the compound described in any of the above-mentioned[1] to [25], or a pharmaceutically acceptable salt thereof, or a solvatethereof to a mammal.[39] A commercial package comprising the pharmaceutical compositiondescribed in the above-mentioned [26] and a written matter associatedtherewith, the written matter stating that the pharmaceuticalcomposition can or should be used for the treatment or prophylaxis of adisease selected from anemia and renal anemia.[40] A kit comprising the pharmaceutical composition described in theabove-mentioned [26] and a written matter associated therewith, thewritten matter stating that the pharmaceutical composition can or shouldbe used for the treatment or prophylaxis of a disease selected fromanemia and renal anemia.

DETAILED DESCRIPTION OF THE INVENTION

The definition of each substituent or each moiety to be used in thepresent specification is as follows.

The “halogen atom” is a fluorine atom, a chlorine atom, a bromine atomor an iodine atom.

The “C₁₋₁₀ alkyl group” is a straight chain or branched chain alkylgroup having a carbon number of 1 to 10, preferably a straight chain orbranched chain alkyl group having a carbon number of 1 to 7. Forexample, a methyl group, an ethyl group, a propyl group, an isopropylgroup, a butyl group, an isobutyl group, a sec-butyl group, a tert-butylgroup, a pentyl group, an isopentyl group, a tert-pentyl group, an1-ethylpropyl group, a neopentyl group, a hexyl group, a 2-ethylbutylgroup, a 3,3-dimethylbutyl group, a 3,3-dimethylpentyl group, a heptylgroup, an octyl group, a nonyl group, a decyl group and the like can bementioned.

The “C₁₋₆ alkyl group” is a straight chain or branched chain alkyl grouphaving a carbon number of 1 to 6, preferably a straight chain orbranched chain alkyl group having a carbon number of 1 to 3. Forexample, those exemplified as the above-mentioned “C₁₋₁₀ alkyl group”and having a carbon number of 1 to 6 can be mentioned.

The “C₁₋₃ alkyl group” is a straight chain or branched chain alkyl grouphaving a carbon number of 1 to 3. For example, those exemplified as theabove-mentioned alkyl group and having a carbon number of 1 to 3 can bementioned.

The “C₆₋₁₄ aryl group” is an aromatic hydrocarbon group having a carbonnumber of 6 to 14. For example, a phenyl group, a naphthyl group, ananthryl group, an indenyl group, an azulenyl group, a fluorenyl group, aphenanthryl group, a pentalenyl group and the like can be mentioned,with preference given to a phenyl group.

The “C₃₋₈ cycloalkyl group” is a saturated cycloalkyl group having acarbon number of 3 to 8, preferably 3 to 5, and, for example, acyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexylgroup, a cycloheptyl group, a cyclooctyl group and the like can bementioned.

The “C₃₋₅ cycloalkyl group” is a saturated cycloalkyl group having acarbon number of 3 to 5. For example, those exemplified as theabove-mentioned “C₃₋₈ cycloalkyl group” and having a carbon number of 3to 5 can be mentioned.

The “C₆₋₁₄ aryl-C₁₋₆ alkyl group” is a C₆₋₁₄ aryl-C₁₋₆ alkyl groupwherein the C₆₋₁₄ aryl moiety thereof is the “C₆₋₁₄ aryl group” definedabove and the C₁₋₆ alkyl moiety thereof is the “C₁₋₆ alkyl group”defined above, with preference given to a C₆₋₁₄ aryl-C₁₋₆ alkyl groupwherein the C₁₋₆ alkyl moiety is a straight chain C₁₋₆ alkyl group.Examples of the C₆₋₁₄ aryl-C₁₋₆ alkyl group include a phenylmethylgroup, a phenylethyl group, a phenylpropyl group, a phenylbutyl group, aphenylpentyl group, a phenylhexyl group, a naphthylmethyl group, anaphthylethyl group, a naphthylpropyl group, a naphthylbutyl group, anaphthylpentyl group, a naphthylhexyl group, an anthrylmethyl group, anindenylmethyl group, an azulenylmethyl group, a fluorenylmethyl group, aphenanthrylmethyl group, a pentalenylmethyl group and the like.

The “C₃₋₈ cycloalkyl-C₁₋₆ alkyl group” is a C₃₋₈ cycloalkyl-C₁₋₆ alkylgroup wherein the C₃₋₈ cycloalkyl moiety thereof is the “C₃₋₈ cycloalkylgroup” defined above and the C₁₋₆ alkyl moiety thereof is the “C₁₋₆alkyl group” defined above. Examples thereof include a cyclopropylmethylgroup, a cyclopropylethyl group, a cyclopropylpropyl group, acyclopropylbutyl group, a cyclopropylpentyl group, a cyclopropylhexylgroup, a cyclobutylmethyl group, a cyclobutylethyl group, acyclobutylpropyl group, a cyclobutylbutyl group, a cyclobutylpentylgroup, a cyclobutylhexyl group, a cyclopentylmethyl group, acyclopentylethyl group, a cyclopentylpropyl group, a cyclopentylbutylgroup, a cyclopentylpentyl group, a cyclopentylhexyl group, acyclohexylmethyl group, a cyclohexylethyl group, a cyclohexylpropylgroup, a cyclohexylbutyl group, a cyclohexylpentyl group, acyclohexylhexyl group, a cycloheptylmethyl group, a cycloheptylethylgroup, a cycloheptylpropyl group, a cycloheptylbutyl group, acycloheptylpentyl group, a cycloheptylhexyl group, a cyclooctylmethylgroup, a cyclooctylethyl group, a cyclooctylpropyl group, acyclooctylbutyl group, a cyclooctylpentyl group, a cyclooctylhexyl groupand the like.

The “C₃₋₈ cycloalkenyl group” is a cycloalkenyl group having a carbonnumber of 3 to 8 and contains at least one, preferably 1 or 2, doublebonds. For example, a cyclopropenyl group, a cyclobutenyl group, acyclopentenyl group, a cyclopentadienyl group, a cyclohexenyl group, acyclohexadienyl group (a 2,4-cyclohexadien-1-yl group, a2,5-cyclohexadien-1-yl group etc.), a cycloheptenyl group, acyclooctenyl group and the like can be mentioned.

The “heteroaryl group” is an aromatic heterocycle having, asring-constituting atom besides carbon atom, 1 to 6 hetero atoms selectedfrom nitrogen atom, oxygen atom and sulfur atom, wherein the number ofring-constituting atom is 3 to 14, including monocycle and fused ring.

The “monocyclic heteroaryl group” is a monocyclic heteroaryl grouppreferably having 1 to 4 hetero atoms and, for example, a thienyl group(e.g., thiophen-2-yl, thiophen-3-yl), a furyl group (e.g., furan-2-yl,furan-3-yl etc.), a pyrrolyl group (e.g., 2-Pyrroline-1-yl group,3-Pyrroline-3-yl etc.), an oxazolyl group (e.g., oxazol-2-yl,oxazol-4-yl, oxazol-5-yl etc.), an isoxazolyl group (e.g.,isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl etc.), a thiazolyl group(e.g., thiazol-2-yl, thiazol-4-yl, thiazol-5-yl etc.), an isothiazolylgroup (e.g., isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl etc.), animidazolyl group (e.g., imidazol-1-yl, 1H-imidazol-2-yl,1H-imidazol-4-yl etc.), a pyrazolyl group (e.g., pyrazol-1-yl,1H-pyrazol-3-yl, 2H-pyrazol-3-yl, 1H-pyrazol-4-yl etc.), an oxadiazolylgroup (e.g., 1,3,4-oxadiazol-2-yl, 1,2,3-oxadiazol-4-yl,1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 1,2,5-oxadiazol-3-yl etc.),a thiadiazolyl group (e.g., 1,3,4-thiadiazol-2-yl,1,2,3-thiadiazol-4-yl, 1,2,3-thiadiazol-5-yl, 1,2,5-thiadiazol-3-yletc.), a triazolyl group (e.g., 1,2,4-triazol-3-yl, 1,2,4-triazol-1-yl,1,2,3-triazol-1-yl, 1,2,3-triazol-2-yl, 1,3,4-triazol-1-yl etc.), atetrazolyl group (e.g., tetrazol-1-yl, tetrazol-2-yl, 1H-tetrazol-5-yl,2H-tetrazol-5-yl etc.), a pyridyl group (e.g., pyridin-2-yl,pyridin-3-yl, pyridin-4-yl etc.), a pyrimidinyl group (e.g.,pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl etc.), a pyridazinylgroup (e.g., pyridazin-3-yl, pyridazin-4-yl etc.), a pyrazinyl group(e.g., pyrazin-2-yl etc.), a triazinyl group (e.g., 1,3,5-triazin-2-yletc.) and the like can be mentioned.

Examples of the “fused heteroaryl group” include a quinolyl group, anisoquinolyl group, a quinazolinyl group, a quinoxalyl group, aphthalazinyl group, a cinnolinyl group, a naphthyridinyl group, anindolyl group, a benzimidazolyl group, an indolinyl group, abenzofuranyl group, a benzothienyl group, a benzoxazolyl group, abenzothiazolyl group, a benzodioxinyl group, a benzothiazolyl group, atetrahydroquinolyl group, a dihydrobenzofuranyl group, adihydrobenzothienyl group, a dihydrobenzodioxinyl group, anindenothiazolyl group, a tetrahydrobenzothiazolyl group, a5,7-dihydropyrrolo[3,4-d]pyrimidinyl group, a6,7-dihydro-5H-cyclopentapyrimidinyl group, an imidazo[2,1-b]thiazolylgroup, a pteridinyl group, a purinyl group and the like.

The “halo-C₁₋₆ alkyl group” is a “C₁₋₆ alkyl group” defined above, whichis substituted by the same or different 1 to 5 halogen atoms, and, forexample, chloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl,bromomethyl, chloroethyl, fluoroethyl, bromoethyl, chloropropyl,fluoropropyl, bromopropyl and the like can be mentioned.

The “group B” includes the following substituent groups (a) to (e).

(a) the “halogen atom” defined above,(b) the “C₁₋₆ alkyl group” defined above,(c) the “C₃₋₈ cycloalkyl group” defined above,(d) a cyano group, and(e) the “halo-C₁₋₆ alkyl group” defined above.

The “C₆₋₁₄ aryl group optionally substituted by the same or different 1to 5 substituents selected from group B” is the “C₆₋₁₄ aryl group”defined above, which is optionally substituted by the same or different1 to 5 substituents, and includes unsubstituted C₆₋₁₄ aryl group. Thesubstituents are the same or different and selected from the “group B”defined above.

The “C₃₋₈ cycloalkyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from group B” is the “C₃₋₈cycloalkyl group” defined above which is optionally substituted by thesame or different 1 to 5 substituents, and includes unsubstituted C₃₋₈cycloalkyl group. The substituents are the same or different andselected from the “group B” defined above.

The “C₃₋₈ cycloalkenyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from group B” is the “C₃₋₈cycloalkenyl group” defined above which is optionally substituted by thesame or different 1 to 5 substituents, and includes unsubstituted C₃₋₈cycloalkenyl group. The substituents are the same or different andselected from the “group B” defined above.

The “heteroaryl group optionally substituted by the same or different 1to 5 substituents selected from group B” is the “heteroaryl group”defined above which is optionally substituted by the same or different 1to 5 substituents, and includes unsubstituted heteroaryl group. Thesubstituents are the same or different and selected from the “group B”defined above.

In the above-mentioned formula [I], preferable groups are as describedbelow.

The partial structural formula:

is a group represented by any of the following formulas:

As the partial structural formula, preferred are groups represented by

and the like.

As the partial structural formula, more preferred is a group representedby

R¹ is

(1) a hydrogen atom,(2) a C₁₋₆ alkyl group,(3) a C₆₋₁₄ aryl group,(4) a C₃₋₈ cycloalkyl group,(5) a C₆₋₁₄ aryl-C₁₋₆ alkyl group, or(6) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group.

R¹ is preferably

(1) a hydrogen atom,(2) a C₁₋₃ alkyl group (e.g., methyl),(3) a C₆₋₁₄ aryl group (e.g., phenyl),(4) a C₃₋₆ cycloalkyl group (e.g., cyclopropyl),(5) a C₆₋₁₄ aryl (e.g., phenyl)-C₁₋₃ alkyl (preferably straight chainC₁₋₃ alkyl, e.g., ethyl) group,(6) a C₃₋₈ cycloalkyl (e.g., cyclohexyl)-C₁₋₃ alkyl (e.g., ethyl) group,or the like.

R¹ is more preferably a hydrogen atom.

R² is

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group,(3) a C₆₋₁₄ aryl group optionally substituted by the same or different 1to 5 substituents selected from the above-mentioned group B,(4) a C₃₋₈ cycloalkyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from the above-mentioned group B,(5) a C₃₋₈ cycloalkenyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from the above-mentioned group B,(6) a heteroaryl group optionally substituted by the same or different 1to 5 substituents selected from the above-mentioned group B (wherein theheteroaryl has, besides carbon atom, 1 to 6 hetero atoms selected fromnitrogen atom, oxygen atom and sulfur atom),(7) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe above-mentioned group B), or(8) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group (wherein C₃₋₈ cycloalkyl isoptionally substituted by the same or different 1 to 5 substituentsselected from the above-mentioned group B).

R² is preferably

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group,(3) a C₆₋₁₄ aryl group optionally substituted by the same or different 1to 5 substituents selected from the above-mentioned group B,(4) a C₃₋₈ cycloalkyl group (e.g., cyclopentyl, cyclohexyl,cycloheptyl),(5) a C₃₋₈ cycloalkenyl group (e.g., cyclohexenyl),(6) a heteroaryl group (preferably monocyclic heteroaryl group, e.g.,thienyl) optionally substituted by the same or different 1 to 5(e.g., 1) substituents selected from the above-mentioned group B

(e.g., (a) a halogen atom (e.g., chlorine atom), and

-   -   (b) a C₁₋₆ alkyl group (e.g., methyl))        (wherein the heteroaryl has, besides carbon atom, 1 to 6 (e.g.,        1 to 4) hetero atoms selected from nitrogen atom, oxygen atom        and sulfur atom (e.g., a sulfur atom)),        (7) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is        optionally substituted by the same or different 1 to 5        substituents selected from the above-mentioned group B), or        (8) a C₃₋₈ cycloalkyl-C₁₋₃ alkyl group (wherein C₃₋₈ cycloalkyl        is optionally substituted by the same or different 1 to 5        substituents selected from the above-mentioned group B).

R² is more preferably

(1) a C₁₋₁₀ alkyl group (e.g., ethyl, propyl, isopropyl, butyl,isobutyl, pentyl, isopentyl, tert-pentyl, hexyl, 1-ethylpropyl,2-ethylbutyl, 3,3-dimethylbutyl, 3,3-dimethylpentyl),(2) a C₆₋₁₄ aryl group (e.g., phenyl) optionally substituted by the sameor different 1 to 5 (e.g., 1 to 3) substituents selected from theabove-mentioned group B

(e.g., (a) a halogen atom (e.g., chlorine atom, fluorine atom),

-   -   (b) a C₁₋₃ alkyl group (e.g., methyl),    -   (c) a C₃₋₅ cycloalkyl group (e.g., cyclopropyl),    -   (d) a cyano group, and    -   (e) a halo-C₁₋₃ alkyl group (e.g., trifluoromethyl)),        (3) a C₆₋₁₄ aryl (e.g., phenyl)-C₁₋₆ alkyl (preferably straight        chain C₁₋₆ alkyl, e.g., methyl, ethyl, propyl) group (the C₆₋₁₄        aryl is optionally substituted by the same or different 1 to 5        (e.g., 1 to 3) substituents selected from the above-mentioned        group B

(e.g., (a) a halogen atom (e.g., chlorine atom, fluorine atom),

-   -   (b) a C₃₋₈ cycloalkyl group (e.g., cyclopropyl), and    -   (c) a halo-C₁₋₃ alkyl group (e.g., trifluoromethyl))), or        (4) a C₃₋₈ cycloalkyl (e.g., cyclopropyl, cyclobutyl,        cyclopentyl, cyclohexyl)-C₁₋₃ alkyl (e.g., methyl, ethyl) group        (the C₃₋₈ cycloalkyl is optionally substituted by the same or        different 1 to 5 substituents selected from the above-mentioned        group B).

R² is still more preferably

(1) a C₁₋₆ alkyl group (e.g., butyl, pentyl, 1-ethylpropyl),(2) phenyl optionally substituted the same or different 1 to 3substituents selected from

-   -   (a) a halogen atom (e.g., chlorine atom, fluorine atom),    -   (b) a C₁₋₃ alkyl group (e.g., methyl),    -   (c) a C₃₋₅ cycloalkyl group (e.g., cyclopropyl), and    -   (d) a halo-C₁₋₃ alkyl group (e.g., trifluoromethyl),        (3) phenylethyl, or        (4) cyclopentylethyl.

R² is particularly preferably butyl, phenylethyl or4-fluoro-3-trifluoromethylphenyl.

In another embodiment of the present invention, R² is preferably

(1) a C₁₋₁₀ alkyl group, or(2) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe above-mentioned group B).

R³ is

(1) a hydrogen atom,(2) a halogen atom,(3) a C₁₋₆ alkyl group,(4) a C₆₋₁₄ aryl group,(5) a C₃₋₈ cycloalkyl group, or(6) a C₆₋₁₄ aryl-C₁₋₆ alkyl group.

R³ is preferably

(1) a hydrogen atom,(2) a halogen atom (e.g., chlorine atom),(3) a C₁₋₆ alkyl group (e.g., ethyl, pentyl),(4) a C₆₋₁₄ aryl group (e.g., phenyl), or(5) a C₆₋₁₄ aryl (e.g., phenyl)-C₁₋₆ alkyl (preferably straight chainC₁₋₆ alkyl, e.g., ethyl) group.

R³ is more preferably a hydrogen atom.

R⁴ and R⁵ are each independently

(1) a hydrogen atom, or(2) a C₁₋₆ alkyl group.

R⁴ and R⁵ are preferably each independently

(1) a hydrogen atom, or(2) a C₁₋₃ alkyl group (e.g., methyl).

R⁴ and R⁵ are more preferably both hydrogen atoms.

In the formula [I], a compound represented by the following formula [Ia]

wherein

the partial structural formula:

is a group represented by

R^(1a) is

(1) a hydrogen atom,(2) a C₁₋₃ alkyl group (e.g., methyl),(3) a C₆₋₁₄ aryl group (e.g., phenyl),(4) a C₃₋₅ cycloalkyl group (e.g., cyclopropyl),(5) a C₆₋₁₄ aryl (e.g., phenyl)-C₁₋₃ alkyl (preferably straight chainC₁₋₃ alkyl, e.g., ethyl) group, or(6) a C₃₋₈ cycloalkyl (e.g., cyclohexyl)-C₁₋₃ alkyl (e.g., ethyl) group;

R^(2a) is

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group,(3) a C₆₋₁₄ aryl group optionally substituted by the same or different 1to 5 substituents selected from the above-mentioned group B,(4) a C₃₋₈ cycloalkyl group (e.g., cyclopentyl, cyclohexyl,cycloheptyl),(5) a C₃₋₈ cycloalkenyl group (e.g., cyclohexenyl),(6) a heteroaryl group (preferably monocyclic heteroaryl group, e.g.,thienyl) optionally substituted by the same or different 1 to 5(e.g., 1) substituents selected from the above-mentioned group B

(e.g., (a) a halogen atom (e.g., chlorine atom), and

-   -   (b) a C₁₋₆ alkyl group (e.g., methyl))

(wherein the heteroaryl has, besides carbon atom, 1 to 6 (e.g., 1 to 4)hetero atoms selected from nitrogen atom, oxygen atom and sulfur atom(e.g., a sulfur atom)),

(7) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe above-mentioned group B), or(8) a C₃₋₈ cycloalkyl-C₁₋₃ alkyl group (wherein C₃₋₈ cycloalkyl isoptionally substituted by the same or different 1 to 5 substituentsselected from the above-mentioned group B);

R^(3a) is

(1) a hydrogen atom,(2) a halogen atom (e.g., chlorine atom),(3) a C₁₋₆ alkyl group (e.g., ethyl, pentyl),(4) a C₆₋₁₄ aryl group (e.g., phenyl), or(5) a C₆₋₁₄ aryl (e.g., phenyl)-C₁₋₆ alkyl (preferably straight chainC₁₋₆ alkyl, e.g., ethyl) group; and

R^(4a) and R^(5a) are each independently

(1) a hydrogen atom, or(2) a C₁₋₃ alkyl group (e.g., methyl)]is more preferable.

As the compound of the present invention, a compound represented by theabove-mentioned formula [Ia], wherein

R^(1a) is a hydrogen atom;

R^(2a) is

(1) a C₁₋₁₀ alkyl group (e.g., ethyl, propyl, isopropyl, butyl,isobutyl, pentyl, isopentyl, tert-pentyl, hexyl, 1-ethylpropyl,2-ethylbutyl, 3,3-dimethylbutyl, 3,3-dimethylpentyl),(2) a C₆₋₁₄ aryl group (e.g., phenyl) optionally substituted by the sameor different 1 to 5 (e.g., 1 to 3) substituents selected from theabove-mentioned group B

(e.g., (a) a halogen atom (e.g., chlorine atom, fluorine atom),

-   -   (b) a C₁₋₃ alkyl group (e.g., methyl),    -   (c) a C₃₋₅ cycloalkyl group (e.g., cyclopropyl),    -   (d) a cyano group, and    -   (e) a halo-C₁₋₃ alkyl group (e.g., trifluoromethyl)),        (3) a C₆₋₁₄ aryl (e.g., phenyl)-C₁₋₆ alkyl (preferably straight        chain C₁₋₆ alkyl, e.g., methyl, ethyl, propyl) group        (the C₆₋₁₄ aryl is optionally substituted by the same or        different 1 to 5 (e.g., 1 to 3) substituents selected from the        above-mentioned group B

(e.g., (a) a halogen atom (e.g., chlorine atom, fluorine atom),

-   -   (b) a C₃₋₈ cycloalkyl group (e.g., cyclopropyl), and    -   (c) a halo-C₁₋₆ alkyl group (e.g., trifluoromethyl))), or        (4) a C₃₋₈ cycloalkyl (e.g., cyclopropyl, cyclobutyl,        cyclopentyl, cyclohexyl)-C₁₋₃ alkyl (e.g., methyl, ethyl) group        (the C₃₋₈ cycloalkyl is optionally substituted by the same or        different 1 to 5 substituents selected from the above-mentioned        group B);

R^(3a) is a hydrogen atom; and

R^(4a) and R^(5a) are both hydrogen atoms;

is more preferable.

In another embodiment of the present invention, from compoundsrepresented by the formula [I], a compound represented by the followingformula [I-1]:

whereinthe partial structural formula:

is a group represented by any of the following formulas:

R¹¹ is

(1) a hydrogen atom,(2) a C₁₋₆ alkyl group (e.g., methyl),(3) a phenyl group,(4) a C₃₋₈ cycloalkyl group (e.g., cyclopropyl),(5) a phenyl-C₁₋₆ alkyl group, or(6) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group;

R²¹ is

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group (e.g., ethyl, n-propyl, isopropyl, n-butyl,isobutyl, n-pentyl, n-hexyl, 1-ethylpropyl, 3-methylbutyl,2,2-dimethylpropyl, 3,3-dimethylbutyl, 2-ethylbutyl,3,3-dimethylpentyl),(3) a phenyl group optionally substituted by the same or different 1 to5 substituents (e.g., fluorine atom, chlorine atom, methyl, cyano,cyclopropyl, trifluoromethyl) selected from m the above-mentioned groupB,(4) a C₃₋₈ cycloalkyl group (e.g., cyclopentyl, cyclohexyl,cycloheptyl),(5) a C₃₋₈ cycloalkenyl group (e.g., cyclohexenyl),(6) a thienyl group optionally substituted by the same or different 1 to5 substituents (e.g., chlorine atom, methyl) selected from theabove-mentioned group B,(7) a phenyl-C₁₋₆ alkyl group (e.g., phenylmethyl, phenylethyl,phenylpropyl) (wherein phenyl is optionally substituted by the same ordifferent 1 to 5 substituents (e.g., fluorine atom, chlorine atom,cyclopropyl, trifluoromethyl) selected from the above-mentioned groupB), or(8) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group (e.g., cyclobutylmethyl,cyclopentylmethyl, cyclohexylmethyl, cyclopropylethyl, cyclobutylethyl,cyclopentylethyl, cyclohexylethyl);

R³¹ is

(1) a hydrogen atom,(2) a halogen atom (e.g., chlorine atom),(3) a C₁₋₆ alkyl group (e.g., ethyl, n-pentyl),(4) a phenyl group,(5) a C₃₋₈ cycloalkyl group, or(6) a phenyl-C₁₋₆ alkyl group (e.g., phenylethyl); andR⁴¹ and R⁵¹ are each independently(1) a hydrogen atom, or(2) a C₁₋₆ alkyl group (e.g., methyl)is preferable.

Of compounds represented by the formula [I-1], a compound wherein

R¹¹ is

(1) a hydrogen atom,(2) a C₁₋₆ alkyl group (e.g., methyl),(3) a phenyl group, or(4) a C₃₋₈ cycloalkyl group (e.g., cyclopropyl);

R²¹ is

(1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group (e.g., ethyl, n-propyl, isopropyl, n-butyl,isobutyl, n-pentyl, n-hexyl, 1-ethylpropyl, 3-methylbutyl,2,2-dimethylpropyl, 3,3-dimethylbutyl, 2-ethylbutyl,3,3-dimethylpentyl).(3) a phenyl group optionally substituted by the same or different 1 to5 substituents (e.g., fluorine atom, chlorine atom, methyl, cyano,cyclopropyl, trifluoromethyl) selected from the above-mentioned group B,(4) a C₃₋₈ cycloalkyl group (e.g., cyclopentyl, cyclohexyl,cycloheptyl),(5) a C₃₋₈ cycloalkenyl group (e.g., cyclohexenyl),(6) a thienyl group optionally substituted by the same or different 1 to5 substituents (e.g., chlorine atom, methyl) selected from theabove-mentioned group B,(7) a phenyl-C₁₋₆ alkyl group (e.g., phenylmethyl, phenylethyl,phenylpropyl) (wherein phenyl is optionally substituted by the same ordifferent 1 to 5 substituents (e.g., fluorine atom, chlorine atom,cyclopropyl, trifluoromethyl) selected from the above-mentioned groupB), or(8) a C₃₋₈ cycloalkyl-C₁₋₅ alkyl group (e.g., cyclobutylmethyl,cyclopentylmethyl, cyclohexylmethyl, cyclopropylethyl, cyclobutylethyl,cyclopentylethyl, cyclohexylethyl);

R³¹ is

(1) a hydrogen atom,(2) a halogen atom (e.g., chlorine atom),(3) a C₁₋₆ alkyl group (e.g., ethyl, n-pentyl),(4) a phenyl group, or(6) a phenyl-C₁₋₆ alkyl group (e.g., phenylethyl);

R⁴¹ and R⁵¹ are each independently

(1) a hydrogen atom, or(2) a C₁₋₆ alkyl group (e.g., methyl),is preferable,

R¹¹ is a hydrogen atom, methyl, phenyl, or cyclopropyl;

R²¹ is a hydrogen atom; ethyl, n-propyl, isopropyl, n-butyl, isobutyl,n-pentyl, n-hexyl, 1-ethylpropyl, 3-methylbutyl, 2,2-dimethylpropyl,3,3-dimethylbutyl, 2-ethylbutyl, 3,3-dimethylpentyl; phenyl optionallysubstituted by the same or different 1 to 5 substituents selected fromfluorine atom, chlorine atom, methyl, cyano, cyclopropyl andtrifluoromethyl; cyclopentyl, cyclohexyl, cycloheptyl; cyclohexenyl;thienyl optionally substituted by the same or different 1 to 5substituents selected from chlorine atom and methyl; phenylmethyl,phenylethyl, phenylpropyl (the phenyl is optionally substituted by thesame or different 1 to 5 substituents selected from fluorine atom,chlorine atom, cyclopropyl and trifluoromethyl); cyclobutylmethyl,cyclopentylmethyl, cyclohexylmethyl, cyclopropylethyl, cyclobutylethyl,cyclopentylethyl, or cyclohexylethyl;

R³¹ is a hydrogen atom, a chlorine atom, ethyl, n-pentyl, phenyl, orphenylethyl; and

R⁴¹ and R⁵¹ is are each independently a hydrogen atom or methyl,

is more preferable.

As the compound of the present invention or a pharmaceuticallyacceptable salt thereof, or a solvate thereof, the compounds describedin Examples 1-122 are preferable, the compounds described in Examples 1,2, 21, 31, 40, 44, 47, 52, 60, 74, 79, 116, 118, 119, 120, 121 and 122are particularly preferable.

A pharmaceutically acceptable salt of the compound represented by theformula [I] may be any salt as long as it forms a nontoxic salt with thecompound of the present invention. Examples thereof include salts withinorganic acids, salts with organic acids, salts with inorganic bases,salts with organic bases, salts with amino acids and the like.

Examples of the salt with inorganic acid include a salt withhydrochloric acid, nitric acid, sulfuric acid, phosphoric acid,hydrobromic acid and the like.

Examples of the salt with organic acid include salts with oxalic acid,maleic acid, citric acid, fumaric acid, lactic acid, malic acid,succinic acid, tartaric acid, acetic acid, trifluoroacetic acid,gluconic acid, ascorbic acid, methanesulfonic acid, benzenesulfonicacid, p-toluenesulfonic acid and the like.

Examples of the salt with inorganic base include sodium salt, potassiumsalt, calcium salt, magnesium salt, ammonium salt and the like.

Examples of the salt with organic base include methylamine,diethylamine, trimethylamine, triethylamine, ethanolamine,diethanolamine, triethanolamine, ethylenediamine,tris(hydroxymethyl)methylamine, dicyclohexylamine,N,N′-dibenzylethylenediamine, guanidine, pyridine, picoline, choline,cinchonine, meglumine and the like.

Examples of the salt with amino acid include salts with lysine,arginine, aspartic acid, glutamic acid and the like.

Each salt can be obtained by reacting a compound represented by theformula [I] with an inorganic base, organic base, inorganic acid,organic acid or amino acid according to a known method.

The “solvate” is a compound represented by the formula [I] or apharmaceutically acceptable salt thereof wherein a molecule of thesolvent is coordinated, and also includes hydrates. As the solvate, apharmaceutically acceptable solvate is preferable and includes, forexample, hydrate, ethanolate, dimethylsulfoxidate and the like of thecompound represented by the formula [I] or a pharmaceutically acceptablesalt thereof. Specific examples thereof include hemihydrate,monohydrate, dihydrate and monoethanolate of the compound represented bythe formula [I], monohydrate of sodium salt, 2/3 ethanolate ofdihydrochloride, and the like of the compound represented by the formula[I].

The solvate of the compound of the present invention or apharmaceutically acceptable salt thereof can be obtained according to amethod known per se.

In addition, the compound represented by the formula [1] or apharmaceutically acceptable salt thereof, or a solvate thereof hasvarious isomers. For example, E form and Z form are present as geometricisomers, when an asymmetric carbon atom is present, enantiomer anddiastereomer are present as stereoisomers based thereon, and when axialchirality is present, stereoisomers based thereon are present. Moreover,tautomers can also be present. Accordingly, the present inventionencompasses all these isomers and mixtures thereof.

In addition, the compound of the present invention or a pharmaceuticallyacceptable salt thereof, or a solvate thereof may be labeled with anisotope (e.g., ³H, ¹⁴C, ³⁵S etc.).

As the compound represented by the formula [I] or a pharmaceuticallyacceptable salt thereof or a solvate thereof, a compound represented bythe formula [I] or a pharmaceutically acceptable salt thereof or asolvate thereof, each of which is substantially purified, is preferable.More preferred is a compound represented by the formula [I] or apharmaceutically acceptable salt thereof or a solvate thereof, each ofwhich is purified to have a purity usable as a pharmaceutical product.

In the present invention, a prodrug of the compound represented by theformula [I] can also be a useful medicament. The “prodrug” is aderivative of the compound of the present invention having a chemicallyor metabolically degradable group which, after administration to thebody, restores to the original compound by, for example, hydrolysis,solvolysis or decomposition under physiological conditions, and showsinherent efficacy. It includes a noncovalent complex, and a salt.Prodrug is utilized for, for example, improvement of absorption on oraladministration, or targeting to a target moiety.

Examples of the modified moiety include, in the compound of the presentinvention, a highly reactive functional group such as a hydroxyl group,a carboxyl group, an amino group and the like.

Specific examples of the hydroxyl-modifying group include an acetylgroup, a propionyl group, an isobutyryl group, a pivaloyl group, apalmitoyl group, a benzoyl group, a 4-methylbenzoyl group, adimethylcarbamoyl group, a dimethylaminomethylcarbonyl group, a sulfogroup, an alanyl group, a fumaryl group and the like. In addition,sodium salt of 3-carboxybenzoyl group, 2-carboxyethylcarbonyl group andthe like can be mentioned.

Specific examples of the carboxyl-modifying group include a methylgroup, an ethyl group, a propyl group, an isopropyl group, a butylgroup, an isobutyl group, a tert-butyl group, a pivaloyloxymethyl group,a carboxymethyl group, a dimethylaminomethyl group, a 1-(acetyloxy)ethylgroup, a 1-(ethoxycarbonyloxy)ethyl group, a1-(isopropyloxycarbonyloxy)ethyl group, a1-(cyclohexyloxycarbonyloxy)ethyl group, a(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl group, a benzyl group, a phenylgroup, an 0-tolyl group, a morpholinoethyl group, anN,N-diethylcarbamoylmethyl group, a phthalidyl group and the like.

Specific examples of the amino-modifying group include a tert-butylgroup, a docosanoyl group, a pivaloyloxymethyl group, an alanyl group, ahexylcarbamoyl group, a pentylcarbamoyl group, a3-methylthio-1-(acetylamino)propylcarbonyl group, a1-sulfo-1-(3-ethoxy-4-hydroxyphenyl)methyl group, a(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl group, a(5-methyl-2-oxo-1,3-dioxol-4-yl)methoxycarbonyl group, atetrahydrofuranyl group, a pyrrolidylmethyl group and the like.

Examples of the “pharmaceutical composition” include oral preparationssuch as tablet, capsule, granule, powder, troche, syrup, emulsion,suspension and the like, and parenteral agents such as externalpreparation, suppository, injection, eye drop, nasal preparation,pulmonary preparation and the like.

The pharmaceutical composition of the present invention is producedaccording to a method known in the art of pharmaceutical preparations,by mixing a compound represented by the formula [I] or apharmaceutically acceptable salt thereof or a solvate thereof with asuitable amount of at least one kind of pharmaceutically acceptablecarrier and the like as appropriate. While the content of the compoundrepresented by the formula [I] or a pharmaceutically acceptable saltthereof, or a solvate thereof in the pharmaceutical composition variesdepending on the dosage form, dose and the like, it is, for example, 0.1to 100 wt % of the whole composition.

Examples of the “pharmaceutically acceptable carrier” include variousorganic or inorganic carrier substances conventionally used aspreparation materials, for example, excipient, disintegrant, binder,glidant, lubricant and the like for solid preparations, and solvent,solubilizing agent, suspending agent, isotonicity agent, bufferingagent, soothing agent and the like for liquid preparations. Wherenecessary, moreover, additives such as preservative, antioxidant,colorant, sweetening agent and the like are used.

Examples of the “excipient” include lactose, sucrose, D-mannitol,D-sorbitol, cornstarch, dextrin, microcrystalline cellulose, crystallinecellulose, carmellose, carmellose calcium, sodium carboxymethyl starch,low-substituted hydroxypropylcellulose, gum arabic and the like.

Examples of the “disintegrant” include carmellose, carmellose calcium,carmellose sodium, sodium carboxymethyl starch, croscarmellose sodium,crospovidone, low-substituted hydroxypropylcellulose,hydroxypropylmethylcellulose, crystalline cellulose and the like.

Examples of the “binder” include hydroxypropylcellulose,hydroxypropylmethylcellulose, povidone, crystalline cellulose, sucrose,dextrin, starch, gelatin, carmellose sodium, gum arabic and the like.

Examples of the “glidant” include light anhydrous silicic acid,magnesium stearate and the like.

Examples of the “lubricant” include magnesium stearate, calciumstearate, talc and the like.

Examples of the “solvent” include purified water, ethanol, propyleneglycol, macrogol, sesame oil, corn oil, olive oil and the like.

Examples of the “solubilizing agents” include propylene glycol,D-mannitol, benzyl benzoate, ethanol, triethanolamine, sodium carbonate,sodium citrate and the like.

Examples of the “suspending agent” include benzalkonium chloride,carmellose, hydroxypropylcellulose, propylene glycol, povidone,methylcellulose, glycerol monostearate and the like.

Examples of the “isotonicity agent” include glucose, D-sorbitol, sodiumchloride, D-mannitol and the like.

Examples of the “buffering agent” include sodium hydrogenphosphate,sodium acetate, sodium carbonate, sodium m citrate and the like.

Examples of the “soothing agent” include benzyl alcohol and the like.

Examples of the “preservative” include ethyl parahydroxybenzoate,chlorobutanol, benzyl alcohol, sodium dehydroacetate, sorbic acid andthe like.

Examples of the “antioxidant” include sodium sulfite, ascorbic acid andthe like.

Examples of the “colorant” include food colors (e.g., Food Color Red No.2 or 3, Food Color Yellow No. 4 or 5 etc.), β-carotene and the like.

Examples of the “sweetening agent” include saccharin sodium, dipotassiumglycyrrhizinate, aspartame and the like.

The compound of the present invention or a pharmaceutically acceptablesalt thereof, or a solvate thereof has an EPO production-inducingactivity due to a prolyl hydroxylase (PHD) inhibitory action, and can beused for the prophylaxis or treatment of various diseases andpathologies (disorders) caused by decreased production of EPO.

As the various diseases and pathologies (disorders) caused by decreasedproduction of EPO, anemia and the like can be mentioned.

In general, anemia includes anemia due to hematopoiesis abnormality inthe bone marrow, anemia due to shortage of iron, vitamin B₁₂ or folicacid, bleeding during accident or operation, anemia associated withchronic inflammation (autoimmune diseases, malignant tumor,chronically-transmitted diseases, plasma cell dyscrasia etc.), anemiaassociated with endocrine diseases (hypothyroidism, autoimmunepolyglandular syndrome, type IA diabetes, dysfunctional uterine bleedingetc.), anemia associated with chronic cardiac failure, anemia associatedwith ulcer, anemia associated with hepatic diseases, senile anemia,drug-induced anemia, renal anemia (anemia associated with renalfailure), anemia associated with chemical therapy, and the like.

Examples of the diseases expected to be improved by inhibiting PHD tostabilize HIF include ischemic cardiac diseases (angina pectoris,myocardial infarction etc.), ischemic cerebrovascular disorders(cerebral infarction, cerebral embolism, transient cerebral ischemicattack etc.), chronic renal failures (ischemic nephropathy, renal tubuleinterstitial disorder etc.), diabetic complications (diabetic woundetc.), cognitive impairments (dementia, Alzheimer's disease, Parkinson'sdisease, Huntington's disease etc.) and the like.

The prolyl hydroxylase (PHD) inhibitor and EPO production-inducing agentof the present invention is preferably used as a therapeutic agent foranemia, more preferably a therapeutic agent for renal anemia.

The pharmaceutical composition of the present invention can beadministered orally or parenterally (e.g., topical, rectal, intravenousadministration etc.) to human as well as mammals other than human (e.g.,mouse, rat, hamster, guinea pig, rabbit, cat, dog, swine, bovine, horse,sheep, monkey etc.). The dose varies depending on the subject ofadministration, disease, symptom, dosage form, administration route andthe like. For example, the daily dose for oral administration to anadult patient (body weight: about 60 kg) is generally within the rangeof about 1 mg to 1 g, based on the compound of the present invention asthe active ingredient. This amount can be administered in one to severalportions.

Since the compound of the present invention or a pharmaceuticallyacceptable salt thereof, or a solvate thereof inhibits PHD and inducesproduction of EPO, it can be used as an active ingredient of atherapeutic agent or prophylactic agent for anemia.

To “inhibit PHD” means to specifically inhibit the function of prolylhydroxylase and eliminate or attenuate the activity. For example, itmeans to specifically inhibit the function as prolyl hydroxylase basedon the conditions in the below-mentioned Experimental Example 1. To“inhibit PHD” preferably means to inhibit human PHD. As a “PHDinhibitor”, preferred is a “human PHD inhibitor”.

To “induce production of EPO” means that the production oferythropoietin in the kidney etc. is promoted. For example, it meansthat the production of erythropoietin is induced based on the conditionsof the below-mentioned Experimental Example 2. To “induce production ofEPO” preferably means to “induce production of human EPO”. An “EPOproduction-inducing agent” is preferably a “human EPOproduction-inducing agent”.

The above-mentioned compound represented by the formula [I] or apharmaceutically acceptable salt thereof, or a solvate thereof can beused in combination with one or a plurality of other medicaments(hereinafter to be also referred to as a concomitant drug) according toa method generally employed in the medical field (hereinafter to bereferred to as combined use).

The administration period of the above-mentioned compound represented bythe formula [I] or a pharmaceutically acceptable salt thereof, or asolvate thereof, and a concomitant drug is not limited, and they may beadministered to an administration subject as combination preparation, orthe both preparations may be administered simultaneously or at givenintervals. In addition, the pharmaceutical composition of the presentinvention and a concomitant drug may be used as a medicament in the formof a kit. The dose of the concomitant drug is similar to theclinically-employed dose and can be appropriately selected according tothe subject of administration, disease, symptom, dosage form,administration route, administration time, combination and the like. Theadministration form of the concomitant drug is not particularly limited,and it only needs to be combined with the compound of the presentinvention or a pharmaceutically acceptable salt thereof, or a solvatethereof.

Examples of the concomitant drug include an agent for the treatmentand/or prophylaxis of anemia and the like, and the compound of thepresent invention can be used in combination.

Examples of the “therapeutic agent and/or prophylaxis agent of anemia”include ferrous citrate, iron sulfate and the like.

As PHD, PHD2 and PHD3 can be mentioned.

Next, the production methods of the compound of the present invention ora pharmaceutically acceptable salt thereof, or a solvate thereof arespecifically explained. However, it is needless to say that the presentinvention is not limited to such production methods. For production ofthe compound of the present invention or a pharmaceutically acceptablesalt thereof, or a solvate thereof, the order of reactions can beappropriately changed. The reaction can be started from the step orsubstitution moiety that seems to be reasonable.

In addition, an appropriate substituent conversion (conversion orfurther modification of substituent) step may be inserted betweenrespective steps. When a reactive functional group is present,protection and deprotection can be appropriately performed. To promoteprogress of the reaction, moreover, a reagent other than the exemplifiedreagent can be used as appropriate. Furthermore, a starting compoundwhose production method is not described is either commerciallyavailable or can be prepared easily by a combination of known syntheticreactions.

The compound obtained in each step can be purified by a conventionalmethod such as distillation, recrystallization, column chromatographyand the like. In some cases, the compound can be applied to the nextstep without isolation and purification.

In the following production method, the “room temperature” means 1-40°C.

Production Method I-1

wherein R^(11a) and R^(11c) are each a carboxyl-protecting group such asa methyl group, an ethyl group, a benzyl group, a tert-butyl group andthe like, R^(11b) is a hydroxyl-protecting group such as an acetylgroup, a benzyl group, a methyl group, an ethyl group, an isopropylgroup, a trimethylsilyl group, a triethylsilyl group, atert-butyldimethylsilyl group, a triisopropylsilyl group, atert-butyldiphenylsilyl group and the like, X^(11a) and R^(11b) are eacha halogen atom such as a chlorine atom, a bromine atom, an iodine atom,a fluorine atom and the like, a leaving group such as ap-toluenesulfonyloxy group, a methanesulfonyloxy group, atrifluoromethanesulfonyloxy group and the like.

Step 1

Compound [I-1-2] can be obtained by subjecting compound [I-1-1] tometalation according to a conventional method, and introducing acarboxyl group using carbon dioxide. Metalation is performed by reactionwith an organic metal reagent such as n-butyllithium, sec-butyllithium,lithium diisopropylamide, lithium bis(trimethylsilyl)amide, sodiumbis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, lithiumamide, sodium amide and the like under low temperature conditions inhexane, benzene, toluene, tetrahydrofuran, diethyl ether, 1,4-dioxaneand the like alone or a mixed solvent thereof, which is followed byreaction with carbon dioxide to give compound [I-1-2].

Step 2

Compound [I-1-3] can be obtained by introducing a protecting group intothe carboxyl group of compound [I-1-2] according to a conventionalmethod. For example, when the protecting group is a tert-butyl group,compound [I-1-3] can be obtained by reaction with tert-butyl2,2,2-trichloroacetimidate under low temperature to heating conditionsin the presence of an acid such as p-toluenesulfonic acid,methanesulfonic acid, boron trifluoride, boron trichloride, borontribromide, aluminum trichloride, hydrogen chloride, hydrogen bromide,phosphoric acid, sulfuric acid, acetic acid, trifluoroacetic acid andthe like in hexane, chloroform, methylene chloride, ethyl acetate,toluene, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane, dimethylsulfoxide, N,N-dimethylformamide, acetonitrile and the like alone or amixed solvent thereof.

Step 3

Compound [I-1-4] can be obtained by introducing a hydroxyl groupprotected by a protecting group represented by R^(11b) into compound[I-1-3] according to a conventional method. For example, when a hydroxylgroup protected by a benzyl group is introduced, compound [I-1-3] isreacted with benzyl alcohol under low temperature to heating conditionsin the presence of a base such as triethylamine, potassiumtert-butoxide, potassium carbonate, sodium hydride, n-butyllithium,lithium diisopropylamide and the like in hexane, dimethyl sulfoxide,N,N-dimethylformamide, acetonitrile, tetrahydrofuran, 1,4-dioxane,1,2-dimethoxyethane, toluene and the like alone or a mixed solventthereof, whereby compound [I-1-4] can be obtained.

Step 4

Compound [I-1-5] can be obtained by reacting compound [I-1-4] withhydrazine monohydrate under low temperature to heating conditions inchloroform, toluene, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane,methanol, ethanol, 2-propanol, dimethyl sulfoxide,N,N-dimethylformamide, acetonitrile, water and the like alone or a mixedsolvent thereof.

Step 5

Compound [I-1-6] can be obtained by reacting compound [I-1-5] with anorthoester compound such as trimethyl orthoformate, triethylorthoformate and the like or formic acid under low temperature toheating conditions in the presence of an acid such as p-toluenesulfonicacid, methanesulfonic acid, boron trifluoride, boron trichloride, borontribromide, hydrogen chloride, hydrogen bromide, phosphoric acid,sulfuric acid and the like in hexane, chloroform, methylene chloride,ethyl acetate, toluene, 1,4-dioxane, tetrahydrofuran,1,2-dimethoxyethane, methanol, ethanol, 2-propanol, dimethyl sulfoxide,N,N-dimethylformamide, acetonitrile and the like alone or a mixedsolvent or without solvent.

Step 6

Compound [I-1-7] can be obtained by performing an endocyclicrearrangement reaction of compound [I-1-6] at room temperature to underheating conditions in the presence of a base such as sodium hydroxide,morpholine, piperidine, pyrrolidine and the like in hexane, chloroform,methylene chloride, ethyl acetate, toluene, 1,2-dimethoxyethane,1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane, methanol, ethanol,2-propanol, dimethyl sulfoxide, N,N-dimethylformamide,N,N-dimethylacetamide, acetonitrile and the like alone or a mixedsolvent thereof.

Step 7

Compound [I-1-8] can be obtained by removing the carboxyl-protectinggroup of compound [I-1-7] according to a conventional method. Forexample, when R^(11a) is a tert-butyl group, compound [I-1-8] can beobtained by reaction with an acid such as p-toluenesulfonic acid,methanesulfonic acid, boron trifluoride, boron trichloride, borontribromide, aluminum trichloride, hydrogen chloride, hydrogen bromide,phosphoric acid, sulfuric acid, acetic acid, trifluoroacetic acid andthe like under low temperature to heating conditions in hexane,chloroform, methylene chloride, ethyl acetate, toluene,1,2-dimethoxyethane, 1,4-dioxane, tetrahydrofuran, methanol, ethanol,2-propanol, dimethyl sulfoxide, N,N-dimethylformamide,N,N-dimethylacetamide, acetonitrile, water and the like alone or a mixedsolvent thereof. When R^(11a) is a methyl group, ethyl group ortert-butyl group, compound [I-1-8] can be obtained by hydrolyzingcompound [I-1-7] under low temperature to heating conditions in thepresence of a base such as sodium hydroxide, potassium hydroxide,potassium carbonate, sodium carbonate, lithium hydroxide and the like ina mixed solvent of water and a solvent such as methanol, ethanol,2-propanol, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane,N,N-dimethylformamide, acetonitrile and the like.

Step 8

Compound [I-1-9] can be obtained by introducing a protecting group intothe carboxyl group of compound [I-1-8] according to a conventionalmethod. For example, when the protecting group is an ethyl group,compound [I-1-9] can be obtained by reacting compound [I-1-8] withN,N-dimethylformamide diethyl acetal under low temperature to heatingconditions in chloroform, methylene chloride, ethyl acetate, toluene,1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane, methanol, ethanol,2-propanol, dimethyl sulfoxide, N,N-dimethylformamide, acetonitrile andthe like alone or a mixed solvent thereof.

Step 7 and step 8 may be omitted. In this case, R

Step 9

Compound [I-1-10] can be obtained by introducing a leaving group ontothe pyridine ring of compound [I-1-9] according to a conventionalmethod. Disubstituted compound [I-1-11] may be obtained. When theleaving group is an iodine atom, compound [I-1-10] and compound [I-1-11]can be obtained by reaction with an organic metal reagent such asn-butyllithium, sec-butyllithium, lithium diisopropylamide, lithiumbis(trimethylsilyl)amide, sodium bis(trimethylsilyl)amide, potassiumbis(trimethylsilyl)amide, lithium amide, sodium amide and the like underlow temperature conditions in hexane, toluene, 1,2-dimethoxyethane,diethyl ether, 1,4-dioxane, tetrahydrofuran and the like alone or amixed solvent thereof to perform metalation, followed by reaction withiodine.

Production method I-2

wherein R^(12a) is a carboxyl-protecting group such as a methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, andother symbols are as defined above. Even when R² of [1-2-1] to [1-2-4]is other than the defined substituents, it can be used as long as thedefined substituent can be finally obtained by appropriate substituentconversion.

Step 1

Compound [I-2-1] can be obtained by introducing substituent R² or aprecursor thereof into compound [I-1-10] according to a conventionalmethod. For example, when R² is a butyl group, compound [I-2-1] can beobtained by reacting compound [I-1-10] with butylboronic acid at roomtemperature to under heating conditions in the presence of a palladiumcatalyst such as [1,1-bis(diphenylphosphino)ferrocene]palladium(II)dichloride, tetrakis(triphenylphosphine)palladium,bis(triphenylphosphine)palladium(II) dichloride, palladiumacetate-triphenylphosphine and the like and a base such as potassiumacetate, potassium carbonate, potassium hydrogen carbonate, sodiumhydrogen carbonate, potassium phosphate, triethylamine,diisopropylethylamine, sodium hydrogenphosphate, cesium carbonate andthe like, by adding a silver salt as necessary such as silver carbonate,silver nitrate, silver(I) oxide and the like in hexane,N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile,1,2-dimethoxyethane, tetrahydrofuran, 1,4-dioxane, toluene, water andthe like alone or a mixed solvent thereof.

Step 2

Compound [I-2-2] can be obtained by removing the carboxyl-protectinggroup of compound [I-2-1] in the same manner as in production methodI-1, step 7.

Step 3

Compound [I-2-3] can be obtained by condensing compound [I-2-2] with aglycine derivative represented by H₂NC(R⁴)(R⁵) COOR^(12a) according to aconventional method. For example, compound [I-2-3] can be obtained bycondensing compound [I-2-2] with a glycine derivative represented byH₂NC(R⁴)(R⁵)COOR^(12a) under low temperature to heating conditions inthe presence of a condensing agent such as dicyclohexylcarbodiimide,1,1′-carbonyldiimidazole, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimideor a salt thereof, diphenylphosphoryl azide and the like and, asnecessary, N-hydroxysuccinimide, 1-hydroxybenzotriazole,dimethylaminopyridine and the like and, as necessary, adding a base suchas potassium carbonate, sodium hydrogen carbonate, cesium carbonate,triethylamine, diisopropylethylamine, morpholine, pyridine and the likein a solvent such as N,N-dimethylformamide, acetonitrile,tetrahydrofuran, chloroform, ethyl acetate, methylene chloride, tolueneand the like.

Step 4

Compound [I-2-4] can be obtained by removing hydroxyl-protecting groupR^(11b) of compound [I-2-3] according to a conventional method. Forexample, when R^(11b) is a benzyl group, compound [I-2-4] can beobtained by hydrogenation under room temperature to heating conditionsunder a hydrogen atmosphere at normal pressure to under pressurizationconditions in the presence of a catalyst such as palladium carbon,palladium hydroxide, platinum oxide, platinum carbon, Raney-nickel andthe like in hexane, methanol, ethanol, 2-propanol, tetrahydrofuran,N,N-dimethylformamide, N,N-dimethylacetamide, ethyl acetate, aceticacid, water and the like alone or a mixed solvent thereof.

Step 5

Compound [I-2-5] can be obtained in the same manner as in productionmethod I-1, step 7, by removing the carboxyl-protecting group ofcompound [I-2-4].

Production Method I-3

wherein even when R² and R³ of [I-3-1] and [I-3-2] are other than thedefined substituents, they can be used as long as the definedsubstituents can be finally obtained by appropriate substituentconversion, and other symbols are as defined above.

Step 1

Compound [I-3-1] can be obtained by introducing substituents R² and R³or a precursor thereof into compound [I-1-11] in the same manner as inproduction method I-2, step 1. For example, when an alkenyl group isintroduced as a precursor of R² and R³, compound [I-3-1] can be obtainedby reacting compound [I-1-11] with alkenylboronic acid in the samemanner as in production method I-2, step 1.

Step 2

Compound [I-3-2] can be obtained by deprotection of R^(11b) of compound[I-3-1] in the same manner as in production method I-2, step 4.

Step 3

Compound [I-3-3] can be obtained by reacting compound [I-3-2] with aglycine derivative represented by H₂NC(R⁴)(R⁵)COOH. For example,compound [I-3-3] can be obtained by reacting compound [I-3-2] with asodium salt of glycine derivative at room temperature to under heatingconditions in hexane, chloroform, methylene chloride, toluene,1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane, methanol, ethanol,2-propanol, 2-methoxyethanol, dimethyl sulfoxide, N,N-dimethylformamide,acetonitrile, water and the like alone or a mixed solvent thereof.

Production Method I-4

wherein even when R³ of [I-4-2] and [I-4-3] is other than the definedsubstituents, it can be used as long as the defined substituents can befinally obtained by appropriate substituent conversion, and othersymbols are as defined above.

Step 1

Compound [I-4-1] can be obtained by stirring compound [I-1-11] under lowtemperature to heating conditions in the presence of a palladiumcatalyst such as [1,1-bis(diphenylphosphino)ferrocene]palladium(II)dichloride, tetrakis(triphenylphosphine)palladium,bis(triphenylphosphine)palladium(II) dichloride, palladiumacetate-triphenylphosphine and the like and a reducing agent such astri-n-butyltin hydride and the like in hexane, chloroform, methylenechloride, ethyl acetate, benzene, toluene, 1,2-dimethoxyethane,1,4-dioxane, tetrahydrofuran, diethyl ether, acetonitrile, water and thelike alone or a mixed solvent thereof.

Step 2

Compound [I-4-2] can be obtained by substitution of X^(11b) of compound[I-4-1] by R³ or a precursor thereof in the same manner as in productionmethod I-2, step 1.

Step 3

Compound [I-4-3] can be obtained by deprotection of R^(11b) of compound[I-4-2] in the same manner as in production method I-2, step 4.

Step 4

Compound [I-4-4] can be obtained by reacting compound [I-4-3] with aglycine derivative represented by H₂NC(R⁴)(R⁵)COOH or a salt with ametal species thereof in the same manner as in production method I-3,step 3.

Production Method I-5

wherein each symbol is as defined above.

Step 1

Compound [I-5-1] can be obtained by introducing substituent R³ intocompound [I-1-10] according to a conventional method. For example, whenR³ is a chloro group, compound [I-5-1] can be obtained by reactingcompound [I-1-10] with a chlorinating agent such as hexachloroethane andthe like under low temperature conditions in the presence of an organicmetal reagent such as n-butyllithium, lithium hexamethyl disilazide,sodium bis(trimethylsilyl)amide, potassium hexamethyl disilazide,lithium diisopropylamide, tert-butoxide and the like in hexane, benzene,toluene, tetrahydrofuran, diethyl ether, 1,4-dioxane and the like aloneor a mixed solvent thereof.

Step 2

Compound [I-5-2] can be obtained by substituting substituent X^(11b) ofcompound [I-5-1] by substituent R² or a precursor thereof in the samemanner as in production method I-2, step 1.

Step 3

Compound [I-5-3] can be obtained by deprotection of R^(ub) of compound[I-5-2] in the same manner as in production method I-2, step 4.

Step 4

Compound [I-5-4] can be obtained by reacting compound [I-5-3] with aglycine derivative represented by H₂NC(R⁴)(R⁵)COOH or a salt with ametal species thereof in the same manner as in production method I-3,step 3.

Production Method I-6

wherein R^(16a) is a hydroxyl-protecting group such as an acetyl group,a benzyl group, a methyl group, an ethyl group, an isopropyl group, atrimethylsilyl group, a triethylsilyl group, a tert-butyldimethylsilylgroup, a triisopropylsilyl group, a tert-butyldiphenylsilyl group andthe like, R^(16b) and R^(16c) are each a carboxyl-protecting group suchas a methyl group, an ethyl group, a benzyl group, a tert-butyl groupand the like, X^(16a) is a halogen atom such as a fluorine atom, achlorine atom, a bromine atom, an iodine atom and the like, or a leavinggroup such as a p-toluenesulfonyloxy group, a methanesulfonyloxy group,a trifluoromethanesulfonyloxy group and the like, and other symbols areas defined above. Even when R² of [1-6-4] to [1-6-10] are other than thedefined substituents, they can be used as long as the definedsubstituents can be finally obtained by appropriate substituentconversion.

Step 1

Compound [I-6-2] can be obtained by introducing a hydroxyl groupprotected by a protecting group R^(16a) into compound [I-6-1] in thesame manner as in production method I-1, step 3.

Step 2

Compound [I-6-3] can be obtained by introducing a carboxyl groupprotected by a protecting group R^(16b) into compound [I-6-2] in thesame manner as in production method I-1, step 1.

Step 3

Compound [I-6-4] can be obtained by introducing substituent R² or aprecursor thereof into compound [I-6-3] in the same manner as inproduction method I-2, step 1.

Step 4

Compound [I-6-5] can be obtained from compound [I-6-4] in the samemanner as in production method I-1, step 4.

Step 5

Compound [I-6-6] can be obtained from compound [I-6-5] in the samemanner as in production method I-1, step 5.

Step 6

Compound [I-6-7] can be obtained from compound [I-6-6] in the samemanner as in production method I-1, step 6.

Step 7

Compound [I-6-8] can be obtained by removing the carboxyl-protectinggroup of compound [I-6-7] in the same manner as in production methodI-1, step 7.

Step 8

Compound [I-6-9] can be obtained by condensing compound [I-6-8] with aglycine derivative represented by H₂NC(R⁴)(R⁵)COOR^(16c) in the samemanner as in production method I-2, step 3.

Step 9

Compound [I-6-10] can be obtained by removing the hydroxyl-protectinggroup R^(16a) of compound [I-6-9] in the same manner as in productionmethod I-2, step 4.

Step 10

Compound [I-6-11] can be obtained by removing the carboxyl-protectinggroup of compound [I-6-10] in the same manner as in production methodI-1, step 7.

Production Method I-7

wherein R^(17a) is a carboxyl-protecting group such as a methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, X^(17a)is a halogen atom such as a fluorine atom, a chlorine atom, a bromineatom, an iodine atom and the like, or a leaving group such as ap-toluenesulfonyloxy group, a methanesulfonyloxy group, atrifluoromethanesulfonyloxy group and the like.

Step 1

Compound [I-7-2] can be obtained by reacting compound [I-7-1] withcyanamide in the presence of an organic metal reagent such as nickel(II)acetylacetonate and the like under low temperature to heating conditionsin hexane, ethyl acetate, chloroform, methylene chloride, toluene,1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane, methanol, ethanol,2-propanol, dimethyl sulfoxide, N,N-dimethylformamide,N-methyl-2-pyrrolidone, acetonitrile, water and the like alone or amixed solvent thereof.

Step 2

Compound [I-7-3] can be obtained by converting the hydroxyl group ofcompound [I-7-2] to a leaving group according to a conventional method.For example, when the leaving group X^(17a) is a chlorine atom, compound[I-7-3] can be obtained by chlorinating compound [I-7-2] with thionylchloride, oxalyl chloride, triphosgene, phosphorus pentachloride,phosphorus oxychloride and the like under low temperature to heatingconditions in hexane, ethyl acetate, acetone, chloroform, methylenechloride, toluene, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane,methanol, ethanol, 2-propanol, dimethyl sulfoxide,N,N-dimethylformamide, 2-pyrrolidone, acetonitrile and the like alone ora mixed solvent thereof or without solvent in the presence of, wherenecessary, a base such as triethylamine, pyridine,4-(dimethylamino)pyridine, N-methylmorpholine, diisopropylethylamine,tetramethylethylenediamine and the like and, where necessary,N,N-dimethylformamide.

Step 3 Compound [I-7-4] can be obtained by reacting compound [I-7-3]with N,N-dimethylformamide dialkyl acetal under low temperature toheating conditions in ethyl acetate, chloroform, toluene, 1,4-dioxane,tetrahydrofuran, 1,2-dimethoxyethane, methanol, ethanol, 2-propanol,dimethyl sulfoxide, N,N-dimethylformamide, acetonitrile and the likealone or a mixed solvent thereof, and then with hydroxylamine or ahydrochloride thereof.

Step 4

Compound [I-7-5] can be obtained by subjecting compound [I-7-4] to adehydrating reaction using polyphosphoric acid, thionyl chloride,phosphorus oxychloride, p-toluenesulfonyl chloride, acetic anhydride,acetyl chloride, trifluoroacetic anhydride and the like under lowtemperature to high temperature conditions in hexane, ethyl acetate,acetone, chloroform, toluene, 1,4-dioxane, tetrahydrofuran,1,2-dimethoxyethane, dimethyl sulfoxide, N,N-dimethylformamide,acetonitrile and the like alone or a mixed solvent thereof.

Production Method I-8

wherein R^(18a) is a hydroxyl-protecting group such as an acetyl group,a benzyl group, a methyl group, an ethyl group, an isopropyl group, atrimethylsilyl group, a triethylsilyl group, a tert-butyldimethylsilylgroup, a triisopropylsilyl group, a tert-butyldiphenylsilyl group andthe like, R^(18b) is a carboxyl-protecting group such as methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, andother symbols are as defined above.

Step 1

Compound [I-8-1] can be obtained by introducing substituent R² or aprecursor thereof into compound [I-7-5] according to a conventionalmethod in the same manner as in production method I-2, step 1.

Step 2

Compound [I-8-2] can be obtained by introducing a hydroxyl groupprotected by a protecting group represented by R^(18a) into compound[I-8-1]. For example, when a hydroxyl group protected by a methyl groupis introduced, compound [I-8-2] can be obtained by reacting compound[I-8-1] with sodium methoxide under low temperature to heatingconditions in hexane, dimethyl sulfoxide, N,N-dimethylformamide,acetonitrile, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane,toluene, methanol, water and the like alone or a mixed solvent thereof,or with a base such as triethylamine, potassium tert-butoxide, sodiummethoxide, potassium carbonate, sodium hydride, n-butyllithium, lithiumdiisopropylamide and the like under low temperature to heatingconditions in methanol alone or a mixed solvent with hexane, dimethylsulfoxide, N,N-dimethylformamide, acetonitrile, tetrahydrofuran,1,4-dioxane, 1,2-dimethoxyethane, toluene and the like.

Step 3

Compound [I-8-3] can be obtained by removing the carboxyl-protectinggroup of compound [I-8-2] in the same manner as in production methodI-1, step 7.

Step 4

Compound [I-8-4] can be obtained by condensing compound [I-8-3] with aglycine derivative represented by H₂NC(R⁴)(R⁵)COOR^(18b) in the samemanner as in production method I-2, step 3.

Step 5

Compound [I-8-5] can be obtained by removing the hydroxyl-protectinggroup R^(18a) and the carboxyl-protecting group R^(18b) of compound[I-8-4] according to a conventional method. For example, when R^(18a) isa methyl group and R^(18b) is a tert-butyl group, compound [I-8-5] canbe obtained by stirring compound [I-8-4] at room temperature to underheating conditions in the presence of an acid such as p-toluenesulfonicacid, methanesulfonic acid, boron trifluoride, boron trifluoride-diethylether complex, boron trichloride, boron tribromide, hydrogen chloride,hydrogen bromide, phosphoric acid, sulfuric acid, acetic acid,trifluoroacetic acid and the like in hexane, ethyl acetate, acetone,chloroform, methylene chloride, ethyl acetate, toluene,1,2-dimethoxyethane, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane,methanol, ethanol, isopropanol, dimethyl sulfoxide,N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, acetic acid,water and the like alone or a mixed solvent thereof.

Production Method I-9

wherein R^(19a) is a carboxyl-protecting group such as a methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, R^(19b)is a metal species forming a salt with carboxylic acid or phenol, suchas lithium, sodium, calcium etc., and other symbols are as definedabove.

Step 1

Compound [I-9-1] can be obtained by removing the carboxyl-protectinggroup of compound [I-8-1] in the same manner as in production methodI-1, step 7.

Step 2

Compound [I-9-2] can be obtained by condensing compound [I-9-1] with aglycine derivative represented by H₂NC(R⁴)(R⁵)COOR^(19a) in the samemanner as in production method I-2, step 3.

Step 3

Compound [I-9-3] can be obtained by reacting compound [I-9-2] with abase. For example, when R^(19b) is sodium, compound [I-9-3] can beobtained by reacting compound [I-9-2] with sodium hydroxide at roomtemperature to under heating conditions in dimethyl sulfoxide,N,N-dimethylformamide, dimethylacetamide, acetonitrile, tetrahydrofuran,1,4-dioxane, 1,2-dimethoxyethane, toluene, methanol, ethanol,2-methoxyethanol, 2-ethoxyethanol, water and the like alone or a mixedsolvent thereof.

Step 4

Compound [I-9-4] can be obtained by reacting compound [I-9-3] with anacid such as acetic acid, p-toluenesulfonic acid, methanesulfonic acid,trifluoroacetic acid, hydrogen chloride, hydrogen bromide, phosphoricacid, sulfuric acid and the like under low temperature to heatingconditions in dimethyl sulfoxide, N,N-dimethylformamide, acetone,acetonitrile, tetrahydrofuran, 1,4-dioxane, 1,2-dimethoxyethane,toluene, methanol, ethanol, 2-methoxyethanol, 2-ethoxyethanol, water andthe like alone or a mixed solvent thereof.

Production Method II-1

wherein R^(21a) is a hydroxyl-protecting group such as a benzyl group,an acetyl group, a methyl group, an ethyl group, an isopropyl group, atrimethylsilyl group, a triethylsilyl group, a tert-butyldimethylsilylgroup, a triisopropylsilyl group, a tert-butyldiphenylsilyl group andthe like, R^(21b) is a carboxyl-protecting group such as methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, andother symbols are as defined above. Even when R² of [II-1-8] to [II-1-9]are other than the defined substituents, they can be used as long as thedefined substituents can be finally obtained by appropriate substituentconversion.

Step 1

Compound [II-1-2] can be, obtained by reacting compound [II-1-1] with2,5-hexanedione under low temperature to heating conditions in thepresence of an acid such as p-toluenesulfonic acid, methanesulfonicacid, boron trifluoride, boron trichloride, boron tribromide, aluminumtrichloride, hydrogen chloride, hydrogen bromide, phosphoric acid,sulfuric acid, sulfamic acid, acetic acid, trifluoroacetic acid and thelike in hexane, chloroform, methylene chloride, ethyl acetate, methanol,ethanol, 2-propanol, toluene, 1,4-dioxane, tetrahydrofuran,1,2-dimethoxyethane, dimethyl sulfoxide, N,N-dimethylformamide,acetonitrile, water and the like alone or a mixed solvent thereof.

Step 2

Compound [II-1-3] can be obtained by introducing a hydroxyl groupprotected by a protecting group represented by R^(21a) into compound[II-1-2] in the same manner as in production method I-1, step 3.

Step 3

Compound [II-1-4] can be obtained by stirring compound [II-1-3] underlow temperature to heating conditions in the presence of a base such astriethylamine, potassium tert-butoxide, potassium carbonate, sodiumhydride, lithium diisopropylamide and the like and hydroxylammoniumchloride in methanol, ethanol, 2-propanol, dimethyl sulfoxide,N,N-dimethylformamide, acetonitrile, water and the like alone or a mixedsolvent thereof.

Step 4

Compound [II-1-4] is reacted with N,N-dimethylformamide dimethyl acetalat room temperature to under heating conditions in ethyl acetate,chloroform, toluene, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane,methanol, ethanol, 2-propanol, dimethyl sulfoxide,N,N-dimethylformamide, acetonitrile and the like alone or a mixedsolvent thereof to give a compound, which is reacted with hydroxylamineor a salt thereof in the presence of a base such as triethylamine,diisopropylethylamine, morpholine, pyridine and the like under lowtemperature to high temperature conditions in hexane, ethyl acetate,acetone, chloroform, toluene, 1,4-dioxane, tetrahydrofuran,1,2-dimethoxyethane, methanol, ethanol, 2-propanol, dimethyl sulfoxide,N,N-dimethylformamide, acetonitrile and the like alone or a mixedsolvent thereof, and reacted with polyphosphoric acid orhydroxylamine-O-sulfonic acid, whereby compound [II-1-5] can beobtained.

Step 5

Compound [II-1-6] can be obtained by introducing a carboxyl group intocompound [II-1-5] in the same manner as in production method I-1, step1.

Step 6

Compound [II-1-7] can be obtained by introducing a protecting groupR^(21b) into the carboxyl group of compound [II-1-6] according to aconventional method. For example, when R^(21b) is an ethyl group,compound [II-1-7] can be obtained by reacting compound [II-1-6] withN,N-dimethylformamide diethyl acetal at room temperature to underheating conditions in hexane, chloroform, methylene chloride, ethylacetate, toluene, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane,dimethyl sulfoxide, N,N-dimethylformamide, acetonitrile and the likealone or a mixed solvent thereof.

Step 7

Compound [II-1-8] can be obtained by introducing a substituent R² or aprecursor thereof into compound [II-1-7] according to a conventionalmethod. For example, when a tert-butylacetylene group is introduced,compound [II-1-8] can be obtained by reacting compound [II-1-7] withtert-butylacetylene at room temperature to under heating conditions inthe presence of a palladium catalyst such as[1,1-bis(diphenylphosphino)ferrocene]palladium(II) dichloride,tetrakis(triphenylphosphine)palladium,bis(triphenylphosphine)palladium(II) dichloride, palladiumacetate-triphenylphosphine and the like, a base such as potassiumacetate, potassium carbonate, potassium hydrogen carbonate, sodiumhydrogen carbonate, potassium phosphate, triethylamine,diisopropylethylamine, sodium hydrogenphosphate, cesium carbonate andthe like and copper iodide in hexane, N,N-dimethylformamide,N,N-dimethylacetamide, acetonitrile, 1,2-dimethoxyethane,tetrahydrofuran, 1,4-dioxane, toluene, water and the like alone or amixed solvent thereof.

Step 8

Compound [II-1-9] can be obtained by deprotection of thehydroxyl-protecting group R^(21a) of compound [II-1-8] in the samemanner as in production method I-2, step 4.

Step 9

Compound [II-1-10] can be obtained from compound [II-1-9] in the samemanner as in production method I-3, step 3.

In this production method, a production method when R¹ is a hydrogenatom has been described. When R¹ is the aforementioned substituent andother than a hydrogen atom, N,N-dimethylformamide dimethyl acetalsubstituted by a desired substituent may be used instead ofN,N-dimethylformamide dimethyl acetal in step 4, and step 5 and thefollowing can be performed by a method similar to the method describedin this production method.

Production Method III-1

wherein R^(31a) and R^(31d) are each a carboxyl-protecting group such asa methyl group, an ethyl group, a benzyl group, a tert-butyl group andthe like, R^(31b) and R^(31c) are each an amino-protecting group such asa benzyloxycarbonyl group, a tert-butoxycarbonyl group, a benzyl groupand the like, X^(31a) and X^(31b) are each a halogen atom such as afluorine atom, a chlorine atom, a bromine atom, an iodine atom and thelike, a leaving group such as a p-toluenesulfonyloxy group, amethanesulfonyloxy group, a trifluoromethanesulfonyloxy group and thelike, and other symbols are as described above.

Step 1

Compound [III-1-2] can be obtained by introducing a leaving groupX^(31b) according to a conventional method into compound [III-1-1]obtained by deprotecting R^(11b) of compound [I-1-4] in the same manneras in production method I-2, step 4. For example, when X^(31b) is abromine atom, compound [III-1-2] can be obtained by reacting compound[III-1-1] with bromine or N-bromosuccinimide under low temperature toheating conditions in hexane, chloroform, methylene chloride, ethylacetate, toluene, tetrahydrofuran, 1,4-dioxane, acetonitrile, water andthe like alone or a mixed solvent thereof.

Step 2

Compound [III-1-3] can be obtained by introducing R^(31b) into compound[III-1-2] according to a conventional method. For example, when R^(31b)is a benzyl group, compound [III-1-3] can be obtained by reactingcompound [III-1-2] with benzyl chloride or benzyl bromide in thepresence of a base such as potassium carbonate, potassium tert-butoxide,sodium hydride, cesium carbonate and the like in ethyl acetate,chloroform, toluene, 1,4-dioxane, tetrahydrofuran, 1,2-dimethoxyethane,dimethyl sulfoxide, N,N-dimethylformamide, acetonitrile, water and thelike alone or a mixed solvent thereof.

Step 3 and Step 4

[III-1-6] can be obtained, by deprotecting R^(31a) of compound [III-1-3]in the same manner as in production method I-1, step 7, converting thecompound to acid chloride according to a conventional method, reactingthe acid chloride with a glycine derivative represented byH₂NC(R⁴)(R⁵)COOR^(31d) in the presence of a base such as triethylamine,diisopropylethylamine, pyridine and the like under low temperature toheating conditions in hexane, chloroform, methylene chloride, ethylacetate, toluene, tetrahydrofuran and the like alone or a mixed solventthereof to give compound [III-1-4], and reacting the compound withcompound [III-1-5] under low temperature to heating conditions in thepresence of a base such as triethylamine, diisopropylethylamine,pyridine and the like in hexane, chloroform, methylene chloride, ethylacetate, toluene, tetrahydrofuran, 1,4-dioxane and the like alone or amixed solvent thereof.

Step 5

Compound [III-1-7] can be obtained from compound [III-1-6] in the samemanner as in production method I-2, step 1.

Step 6

Compound [III-1-8] can be obtained by deprotection of R^(31b) ofcompound [III-1-7] in the same manner as in production method I-2, step4.

Step 7

Compound [III-1-9] can be obtained by removing the amino-protectinggroup R^(31c) of compound [III-1-8] according to a conventional method.For example, when R^(31c) is a tert-butoxycarbonyl group, compound[III-1-9] can be obtained by stirring under low temperature to roomtemperature conditions in the presence of an acid such as hydrogenchloride, sulfuric acid, hydrogen bromide, phosphoric acid, acetic acid,trifluoroacetic acid and the like in hexane, chloroform, methylenechloride, ethyl acetate, toluene, methanol, ethanol, 2-propanol,tetrahydrofuran, 1,4-dioxane, acetonitrile, water and the like alone ora mixed solvent thereof.

Step 8

Compound [III-1-10] can be obtained from compound [III-1-9] in the samemanner as in production method I-1, step 5.

Step 9

Compound [III-1-11] can be obtained by removing the carboxyl-protectinggroup of compound [III-1-10] in the same manner as in production methodI-1, step 7.

Production Method III-2

wherein R^(32a) is a carboxyl-protecting group such as a methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, andother symbols are as defined above.

Step 1

Compound [III-2-1] can be obtained from compound [I-6-5] in the samemanner as in production method I-1, step 5.

Step 2

Compound [III-2-2] can be obtained by removing the carboxyl-protectinggroup of compound [III-2-1] in the same manner as in production methodI-1, step 7.

Step 3

Compound [III-2-3] can be obtained by condensing compound [III-2-2] witha glycine derivative represented by H₂NC(R⁴)(R⁵)COOR^(32a) in the samemanner as in production method I-2, step 3.

Step 4

Compound [III-2-4] can be obtained by deprotection of R^(16a) ofcompound [III-2-3] in the same manner as in production method I-2, step4.

Step 5

Compound [III-2-5] can be obtained by removing the carboxyl-protectinggroup of compound [III-2-4] in the same manner as in production methodI-1, step 7.

Production Method IV-1

wherein R^(41a) is a hydroxyl-protecting group such as an acetyl group,a benzyl group, a methyl group, an ethyl group, an isopropyl group, atrimethylsilyl group, a triethylsilyl group, a tert-butyldimethylsilylgroup, a triisopropylsilyl group, a tert-butyldiphenylsilyl group andthe like, R^(41b) is a carboxyl-protecting group such as a methyl group,an ethyl group, a benzyl group, a tert-butyl group and the like, X^(41a)and X^(41b) are each a halogen atom such as a chlorine atom, a bromineatom, an iodine atom and the like, a leaving group such as ap-toluenesulfonyloxy group, a methanesulfonyloxy group, atrifluoromethanesulfonyloxy group, a p-toluenesulfonyl group, amethanesulfonyl group and the like, and other symbols are as definedabove.

Step 1

Compound [IV-1-2] can be obtained by converting the leaving groupX^(41a) of compound [IV-1-1] to a formyl group according to aconventional method. Compound [IV-1-2] can be obtained by reactingcompound [IV-1-1] with an organic metal reagent such as n-butyllithium,sec-butyllithium, lithium diisopropylamide, lithiumbis(trimethylsilyl)amide, sodium bis(trimethylsilyl)amide, potassiumbis(trimethylsilyl)amide, lithium amide, sodium amide and the like underlow temperature conditions in hexane, benzene, toluene, tetrahydrofuran,diethyl ether, 1,4-dioxane and the like alone or a mixed solventthereof, and then with N,N-dimethylformamide.

Step 2 and Step 3

Compound [IV-1-4] can be obtained by reacting compound [IV-1-2] withhydrazine having a leaving group X^(41b) under room temperature to underheating conditions in ethyl acetate, chloroform, toluene, 1,4-dioxane,tetrahydrofuran, 1,2-dimethoxyethane, methanol, ethanol, isopropanol,dimethyl sulfoxide, N,N-dimethylformamide, acetonitrile and the likealone or a mixed solvent thereof, then adding a base such as morpholine,piperidine, pyrrolidine and the like, and stirring the mixture.

Step 4

Compound [IV-1-5] can be obtained from compound [IV-1-4] in the samemanner as in production method I-1, step 1.

Step 5

Compound [IV-1-6] can be obtained by condensing compound [IV-1-5] with aglycine derivative in the same manner as in production method I-2, step3.

Step 6

Compound [IV-1-7] can be obtained by deprotection of R^(41a) of compound[IV-1-6] in the same manner as in production method I-2, step 4.

Step 7

Compound [IV-1-8] can be obtained by removing the carboxyl-protectinggroup of compound [IV-1-7] in the same manner as in production methodI-1, step 7.

In this production method, a production method when R¹ is a hydrogenatom has been described. When R¹ is the aforementioned substituent andother than a hydrogen atom, N,N-dimethylformamide substituted by adesired substituent may be used instead of N,N-dimethylformamide in step1, and step 2 and the following can be performed by a method similar tothe method described in this production method.

EXAMPLES

Now the production method of the compound of the present invention or apharmaceutically acceptable salt thereof, or a solvate thereof isspecifically explained by way of Examples. However, the presentinvention is not limited by the Examples.

Example 1 Production of{[5-(4-fluoro-3-trifluoromethylphenyl)-7-hydroxy[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl]amino}aceticacid hydrochloride Step 1-1

Under a nitrogen stream, diisopropylamine (198 ml) and tetrahydrofuran(1000 ml) were mixed, and n-butyllithium (2.76M, 500 ml) was addeddropwise under cooling in dry ice/hexane bath. After stirring in the dryice/hexane bath for 1 hr, 2,4-dichloropyridine was added dropwise. Afterstirring under cooling in the dry ice/hexane bath for 1 hr, carbondioxide was blown until the temperature rise ceased while preventing atemperature of not less than −60° C. Carbon dioxide was further blownfor 30 min under cooling in the dry ice/hexane bath, and 4N hydrochloricacid (1000 ml) was added dropwise. The aqueous layer was extracted twicewith ethyl acetate (each 1000 ml, 500 ml). The organic layers werecombined, dried over sodium sulfate, filtered, and concentrated underreduced pressure. The obtained solid was slurried in hexane to give thecompound described in the above-mentioned scheme (243 g, 96%).

¹H-NMR (DMSO-D₆) δ: 7.74 (1H, d, J=5.6 Hz), 8.47 (1H, d, J=5.6 Hz),14.53 (1H, br s).

Step 1-2

The compound (234 g) obtained in step 1-1 and tetrahydrofuran (1200 ml)were mixed, and boron trifluoride-diethyl ether complex (8 ml) wasadded. Then, tert-butyl 2,2,2-trichloroacetimidate (361 ml) was addeddropwise under ice-cooling. To this reaction mixture were addedsaturated aqueous sodium hydrogen carbonate solution (1200 ml) and water(1200 ml), and the aqueous layer was extracted with ethyl acetate (1200ml). The organic layer was washed with saturated brine, dried oversodium sulfate, filtered, and concentrated under reduced pressure.Hexane (1800 ml) was added to the obtained residue. Insoluble materialwas filtered off, and the filtrate was concentrated under reducedpressure to give the compound described in the above-mentioned scheme(326 g) as a crude product.

¹H-NMR (CDCl₃) δ: 1.63 (9H, s), 7.31 (1H, d, J=5.2 Hz), 8.31 (1H, d,J=5.2 Hz).

Step 1-3

Under a nitrogen stream, sodium hydride (60% oil suspension) (58 g) andN,N-dimethylformamide (1000 ml) were mixed under ice-cooling. Thecompound (326 g) obtained in step 1-2 was dissolved inN,N-dimethylformamide (300 ml) and added thereto. To this mixture wasadded a mixture of benzyl alcohol (136 ml) and N,N-dimethylformamide(200 ml). After stirring under ice-cooling for 15 min, sodium hydride(60% oil suspension) (5.2 g) was added. After stirring under ice-coolingfor 20 min more, water (3000 ml) was added and the precipitated solidwas filtered, and the filtrate was dried under reduced pressure at 50°C. overnight. The solid was purified by column chromatography (eluent:hexane/ethyl acetate=10/1-ethyl acetate alone). The obtained solid wasfurther slurried in hexane to give the object product. The filtrate atthis time was concentrated, purified by column chromatography, andslurried in hexane to give the object product. They were combined togive the compound described in the above-mentioned scheme (334 g, 83%yield).

¹H-NMR (CDCl₃) δ: 1.55 (9H, s), 5.17 (2H, s), 6.83 (1H, d, J=6.0 Hz),7.32-7.42 (5H, m), 8.24 (1H, d, J=6.0 Hz).

Step 1-4

The compound (167 g) obtained in step 1-3, hydrazine monohydrate (127ml) and 1,4-dioxane (1200 ml) were mixed, and the reaction mixture wasstirred at 94° C. for 17 hr. After cooling to room temperature, ethylacetate (1700 ml) was added, and the mixture was washed successivelywith saturated aqueous sodium hydrogen carbonate solution (500 ml)/water(500 ml), saturated aqueous sodium hydrogen carbonate solution (250ml)/water (250 ml), and saturated aqueous sodium hydrogen carbonatesolution (200 ml)/water (200 ml). The organic layer was dried oversodium sulfate, filtered, and concentrated under reduced pressure. Byperforming the operation twice, the compound described in theabove-mentioned scheme (266 g) was obtained as a crude product.

¹H-NMR (CDCl₃) δ: 1.42 (9H, s), 3.98 (2H, br s), 5.09 (2H, s), 6.32 (1H,d, J=5.6 Hz), 7.28-7.45 (5H, m), 7.96 (1H, br s), 8.08 (1H, d, J=5.6Hz).

Step 1-5

The compound (266 g) obtained in the same manner as in step 1-4 andtrimethyl orthoformate (1000 ml) were mixed, p-toluenesulfonic acidmonohydrate (80 g) was added, and the mixture was stirred at 56° C. for1 hr. The reaction mixture was concentrated under reduced pressure, andthe obtained residue was slurried in hexane/ethyl acetate=2/1.Furthermore, the residue was slurried in saturated aqueous sodiumhydrogen carbonate solution/water=1/1 to give the compound described inthe above-mentioned scheme (209 g, 76%).

¹H-NMR (DMSO-D₆) δ: 1.49 (9H, s), 5.36 (2H, s), 7.22 (1H, d, J=7.6 Hz),7.32-7.50 (5H, m), 8.62 (1H, d, J=7.6 Hz), 9.13 (1H, s).

Step 1-6

The compound (200 g) obtained in step 1-5 and ethyl acetate (600 ml)were mixed, morpholine (160 ml) was added and the mixture was stirred at74° C. for 3 hr. The mixture was allowed to cool to room temperature,and water (600 ml) was added. The aqueous layer was extracted with ethylacetate (400 ml), the organic layers were combined and washedsuccessively with 5% aqueous potassium hydrogensulfate solution (600 ml)and saturated brine. The organic layer was dried over sodium sulfate,filtered, and concentrated under reduced pressure to give the compounddescribed in the above-mentioned scheme (194 g, 97%).

¹H-NMR (CDCl₃) δ: 1.59 (9H, s), 5.28 (2H, s), 6.85 (1H, d, J=7.6 Hz),7.33-7.46 (5H, m), 8.29 (1H, s), 8.50 (1H, d, J=7.6 Hz).

Step 1-7

Under a nitrogen stream, the compound (194 g) obtained in step 1-6 andtetrahydrofuran (600 ml) were mixed under cooling in a dry ice/hexanebath, and a solution of iodine (151 g) in tetrahydrofuran (500 ml) wasadded dropwise. To this mixture was added dropwise 1.6M lithiumbis(trimethylsilyl)amide (788 ml) while preventing a temperature of notless than −60° C. After stirring under cooling in a dry ice/hexane bathfor 2 hr, 4N hydrochloric acid-ethyl acetate (315 ml) was added dropwisewhile preventing a temperature of not less than −60° C. To this reactionmixture were added sodium sulfite (76 g), saturated aqueous ammoniumchloride solution (1000 ml), water (800 ml) and hexane/ethyl acetate=1/1(1000 ml). The organic layer was washed successively with saturatedaqueous sodium hydrogen carbonate solution (500 ml) and saturated brine(800 ml), dried over sodium sulfate, filtered, and concentrated underreduced pressure to give a crude product. The crude product was slurriedin hexane to give the compound described in the above-mentioned scheme(188 g, 70%).

¹H-NMR (DMSO-D₆) δ: 1.46 (9H, s), 5.39 (2H, s), 7.33-7.51 (5H, m), 7.87(1H, s), 8.43 (1H, s).

Step 1-8

The compound (60 g) obtained in step 1-7,4-fluoro-3-(trifluoromethyl)phenylboronic acid (29 g),[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloridedichloromethane complex (1:1) (5.4 g), potassium phosphate (113 g) and1,2-dimethoxyethane (600 ml) were mixed, and the mixture was stirred at80° C. for 1 hr. Water was added to the reaction mixture, and themixture was extracted with ethyl acetate. The organic layer was washedwith saturated brine, dried over anhydrous magnesium sulfate, filteredand concentrated under reduced pressure. The obtained solid was purifiedby column chromatography (eluent: chloroform/ethyl acetate=10/1) to givea crude product of the compound described in the above-mentioned scheme.This was slurried in diisopropyl ether/hexane=1/1 (500 ml) to give thecompound described in the above-mentioned scheme (45 g, 70%).

¹H-NMR (CDCl₃) δ: 1.61 (9H, s), 5.33 (2H, s), 6.88 (1H, s), 7.35-7.48(6H, m), 8.04 (1H, dd, J=6.7, 2.1 Hz), 8.11-8.15 (1H, m), 8.31 (1H, s).

Step 1-9

The compound (45 g) obtained in step 1-8 and 1,4-dioxane (450 ml) weremixed, and 4N aqueous sodium hydroxide solution (116 ml) was added atroom temperature. After stirring at 100° C. for 17 hr, the reactionmixture was concentrated under reduced pressure. Water (450 ml) wasadded thereto, and the mixture was neutralized with 6N hydrochloric acid(77 ml) under ice-cooling, and the precipitated solid was collected byfiltration to give the compound described in the above-mentioned scheme(43 g).

¹H-NMR (DMSO-D₆) δ: 5.51 (2H, s), 7.34-7.38 (1H, m), 7.41-7.45 (2H, m),7.50-7.52 (2H, m), 7.63 (1H, s), 7.80 (1H, dd, J=10.5, 8.9 Hz),8.40-8.48 (2H, m), 8.48 (1H, s).

Step 1-10

The compound (43 g) obtained in step 1-9, glycine ethylesterhydrochloride (15 g), 1-hydroxybenzotriazole hydrate (17 g) andN,N-dimethylformamide (430 ml) were mixed, and triethylamine (15 ml) and1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (21 g) wereadded at room temperature. After stirring at room temperature for 1 hr,water (860 ml) and saturated aqueous sodium hydrogen carbonate solution(215 ml) were added, and the precipitated solid was collected byfiltration to give the compound described in the above-mentioned scheme(43 g, 84%).

¹H-NMR (CDCl₃) δ: 1.33 (3H, t, J=7.1 Hz), 4.28 (2H, q, J=7.1 Hz), 4.35(2H, d, J=4.8 Hz), 5.47 (2H, s), 6.95 (1H, s), 7.32-7.43 (4H, m), 7.54(2H, d, J=7.3 Hz), 8.01 (1H, dd, J=6.4, 2.0 Hz), 8.10-8.14 (1H, m), 8.31(1H, s), 9.72 (1H, t, J=4.8 Hz).

Step 1-11

The compound (43 g) obtained in step 1-10 and trifluoroacetic acid (430ml) were mixed and, after stirring at 80° C. for 6 hr, the reactionmixture was concentrated under reduced pressure. Methanol (86 ml) andwater (430 ml) were added to the residue, and the mixture was stirred atroom temperature for 30 min, and the precipitated solid was collected byfiltration. This was purified by column chromatography (eluent:chloroform/ethyl acetate=10/1) to give the compound described in theabove-mentioned scheme (28 g, 79%).

¹H-NMR (CDCl₃) δ: 1.34 (3H, t, J=7.3 Hz), 4.30 (2H, q, J=7.3 Hz), 4.33(2H, d, J=5.2 Hz), 6.87 (1H, s), 7.41 (1H, dd, J=9.7, 8.9 Hz), 8.16-8.20(1H, m), 8.24 (1H, dd, J=6.9, 2.4 Hz), 8.26 (1H, s), 10.15 (1H, t, J=5.2Hz), 14.13 (1H, s).

Step 1-12

The compound (27 g) obtained in step 1-11 and 2-propanol (540 ml) weremixed, and 4N aqueous lithium hydroxide solution (64 ml) was added atroom temperature. After stirring at 70° C. for 1 hr, 6N hydrochloricacid (43 ml) was added. This was allowed to gradually cool with stirringand crystals were precipitated at 37° C. Water (270 ml) was added andthe crystals were collected by filtration to give the compound describedin the above-mentioned scheme (22 g, 87%).

¹H-NMR (DMSO-D₆) δ: 4.24 (2H, d, J=5.6 Hz), 7.30 (1H, s), 7.77 (1H, dd,J=10.5, 9.3 Hz), 8.36-8.40 (1H, m), 8.47 (1H, d, J=6.9 Hz), 8.60 (1H,s), 9.97 (1H, br s), 14.38 (1H, br s).

The obtained compound was converted to hydrochloride according to aconventional method to give the compound of Example 1.

¹H-NMR (DMSO-D₆) δ: 4.25 (d, 2H, J=5.6 Hz), 7.31 (s, 1H), 7.73-7.82 (m,1H), 8.34-8.43 (m, 1H), 8.43-8.51 (m, 1H), 8.61 (s, 1H), 9.99 (t, 1H,J=5.6 Hz).

Example 2 Production of[(7-hydroxy-5-phenethyl[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid hydrochloride Step 2-1

The compound (5.00 g) obtained in step 1-7, toluene (35 ml) andphenylacetylene (1.34 ml) were mixed, andbis(triphenylphosphine)palladium dichloride (0.233 g), copper iodide(0.063 g) and triethylamine (1.85 ml) were successively added underice-cooling. After stirring at room temperature for 2 hr, 5% aqueousammonia (35 ml) was added to the reaction mixture. The organic layer wasfurther washed successively with 5% aqueous ammonia, saturated aqueousammonium chloride solution and saturated brine, and dried over anhydrousmagnesium sulfate. After filtration, the filtrate was concentrated underreduced pressure, and the obtained residue was purified by columnchromatography (eluent: hexane/ethyl acetate=3/1-1/1). The obtainedcompound was slurried in hexane to give the compound described in theabove-mentioned scheme (3.84 g, 82%).

¹H-NMR (DMSO-D₆) δ: 1.48 (9H, s), 5.42 (2H, s), 7.36 (1H, tt, J=7.1, 1.8Hz), 7.40-7.45 (2H, m), 7.48 (2H, dt, J=7.0, 1.9 Hz), 7.51-7.58 (3H, m),7.72 (2H, dd, J=7.7, 1.6 Hz), 7.78 (1H, s), 8.49 (1H, s).

Step 2-2

The compound (3.84 g) obtained in step 2-1, toluene (29 ml) and ethylacetate (9.5 ml) were mixed, a mixture of methanesulfonic acid (2.34 ml)and ethyl acetate (2.34 ml) was added dropwise over 10 min at roomtemperature with stirring. After stirring at room temperature for 3 hr,ethyl acetate (9.5 ml) was added to the reaction mixture, and the solidwas collected by filtration to give the compound described in theabove-mentioned scheme (4.94 g, 98%).

¹H-NMR (DMSO-D₆) δ: 2.38 (6H, s), 5.48 (2H, s), 7.37 (1H, tt, J=7.2, 1.7Hz), 7.41-7.45 (2H, m), 7.48-7.52 (2H, m), 7.53-7.62 (3H, m), 7.71-7.75(2H, m), 7.86 (1H, s), 8.67 (1H, s).

Step 2-3

The compound (4.94 g) obtained in step 2-2 and N,N-dimethylformamide (30ml) were mixed at room temperature, and water (50 ml) was added dropwiseat 0° C. over 10 min. The precipitated solid was collected by filtrationto give the compound described in the above-mentioned scheme (3.20 g,98%).

¹H-NMR (DMSO-D₆) δ: 5.45 (2H, s), 7.36 (1H, tt, J=7.4, 2.1 Hz), 7.43(2H, t, J=7.3 Hz), 7.49 (2H, d, J=7.5 Hz), 7.52-7.60 (3H, m), 7.72 (2H,dd, J=6.7, 1.9 Hz), 7.78 (1H, s), 8.51 (1H, s), 13.59 (1H, s).

Step 2-4

The compound (3.20 g) obtained in step 2-3 was reacted with glycineethyl ester hydrochloride (1.33 g) by a method similar to Example 1,step 1-10, to give the compound described in the above-mentioned scheme(3.38 g, 81%).

¹H-NMR (DMSO-D₆) δ: 1.21 (3H, t, J=7.1 Hz), 4.10 (2H, d, J=5.7 Hz), 4.13(2H, q, J=7.5 Hz), 5.44 (2H, s), 7.34 (1H, tt, J=7.2, 1.7 Hz), 7.38-7.43(2H, m), 7.52-7.58 (5H, m), 7.71-7.74 (2H, m), 7.75 (1H, s), 8.52 (1H,s), 9.18 (1H, t, J=5.8 Hz).

Step 2-5

To a solution of the compound (3.38 g) obtained in step 2-4 intetrahydrofuran (34 ml) and methanol (17 ml) was added 5% palladiumcarbon (0.34 g), and the mixture was stirred under a hydrogen atmosphereand normal pressure for 4 hr. The reaction mixture was filtered throughcelite, and concentrated under reduced pressure. The obtained residuewas purified by column chromatography (eluent:chloroform/methanol=20/0-20/1) and slurried in hexane/diisopropylether=1/1 to give the compound described in the above-mentioned scheme(2.29 g, 83%).

¹H-NMR (DMSO-D₆) δ: 1.23 (3H, t, J=7.2 Hz), 3.12 (2H, t, J=7.8 Hz), 3.41(2H, t, J=7.9 Hz), 4.17 (2H, q, J=7.1 Hz), 4.29 (2H, d, J=5.7 Hz), 6.82(1H, s), 7.18-7.32 (5H, m), 8.58 (1H, s), 9.87 (1H, t, J=5.6 Hz), 14.12(1H, s).

Step 2-6

The compound (2.28 g) obtained in step 2-5 was hydrolyzed by a methodsimilar to step 1-12, and the obtained compound was converted tohydrochloride according to a conventional method to give the titlecompound (2.16 g).

1H-NMR (DMSO-D6) δ: 3.12 (t, 2H, J=7.8 Hz), 3.41 (t, 2H, J=7.8 Hz), 4.21(d, 2H, J=5.6 Hz), 6.81 (s, 1H), 7.14-7.33 (m, 5H), 8.60 (s, 1H), 9.85(t, 1H, J=5.6 Hz).

Example 3 production of[(5-butyl-7-hydroxy[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid hydrochloride Step 3-1

The compound (0.2 g) obtained in step 1-7,[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloridedichloromethane complex (1:1) (0.011 g), butylboronic acid (0.050 g),silver(I) oxide (0.12 g), potassium carbonate (0.15 g) andtetrahydrofuran (1.6 ml) were mixed, and the mixture was stirred at 80°C. for 40 hr. Insoluble material was filtered off, and the filtrate wasconcentrated under reduced pressure. The residue was purified by columnchromatography (eluent: hexane/ethyl acetate=8/2-6/4) to give thecompound described in the above-mentioned scheme (0.13 g, 77%).

¹H-NMR (DMSO-D₆) δ: 0.91 (t, 3H, J=7.7 Hz), 1.28-1.39 (m, 2H), 1.48 (s,9H), 1.71-1.81 (m, 2H), 3.11 (t, 2H, J=7.7 Hz), 5.38 (s, 2H), 7.23 (s,1H), 7.32-7.51 (m, 5H), 8.39 (s, 1H).

Step 3-2

The carboxyl-protecting group of the compound (53.7 g) obtained in step3-1 was removed in the same manner as in step 2-2 to give a carboxylicacid form as a mixture (69.8 g, 80%) with methanesulfonic acid (290 mol%). The mixture was treated in the same manner as in step 2-3 to givethe compound described in the above-mentioned scheme as a mixture (42.8g, 99%) with methanesulfonic acid (50 mol %).

¹H-NMR (DMSO-D₆) δ: 0.91 (t, 3H, J=7.7 Hz), 1.29-1.40 (m, 2H), 1.71-1.80(m, 2H), 2.34 (s, 1.5H), 3.14 (t, 2H, J=7.7 Hz), 5.47 (s, 2H), 7.32-7.45(m, 4H), 7.48-7.53 (m, 2H), 8.73 (s, 1H).

Step 3-3

By a method similar to step 1-10, the compound (42.8 g) obtained in step3-2 was reacted with glycine ethyl ester hydrochloride (19.3 g) to givethe compound described in the above-mentioned scheme (43.5 g, 92%).

¹H-NMR (CDCl₃) δ: 0.94 (t, 3H, J=7.5 Hz), 1.31 (t, 3H, J=7.1 Hz),1.34-1.43 (m, 2H), 1.70-1.79 (m, 2H), 3.11 (t, 2H, J=7.5 Hz), 4.26 (q,2H, J=7.1 Hz), 4.33 (d, 2H, J=5.2 Hz), 5.41 (s, 2H), 6.69 (s, 1H),7.29-7.55 (m, 5H), 8.28 (s, 1H), 9.77 (t, 1H, J=5.2 Hz).

Step 3-4

In the same manner as in step 2-5, the compound described in theabove-mentioned scheme (5.0 g, 90%) was obtained from the compound (7.2g) obtained in step 3-3.

¹H-NMR (DMSO-D₆) δ: 0.93 (t, 3H, J=7.5 Hz), 1.22 (t, 3H, J=7.3 Hz),1.33-1.44 (m, 2H), 1.71-1.81 (m, 2H), 3.09 (t, 2H, J=7.5 Hz), 4.16 (q,2H, J=7.3 Hz), 4.29 (d, 2H, J=5.6 Hz), 6.85 (s, 1H), 8.54 (s, 1H), 9.88(br s, 1H), 14.14 (s, 1H).

Step 3-5

In the same manner as in step 1-12, the compound described in theabove-mentioned scheme (4.56 g) was obtained from the compound (4.94 g)obtained in step 3-4.

¹H-NMR (DMSO-D₆) δ: 0.93 (t, 3H, J=7.5 Hz), 1.33-1.44 (m, 2H), 1.71-1.80(m, 2H), 3.10 (t, 2H, J=7.5 Hz), 4.20 (d, 2H, J=5.2 Hz), 6.85 (s, 1H),8.55 (s, 1H), 9.84 (br s, 1H), 14.26 (br s, 1H).

Step 3-6

The compound (4.56 g) obtained in step 3-5 and 4N hydrochloricacid/ethyl acetate solution (91 ml) were mixed, and the mixture wasstirred at room temperature for 1.5 hr. The reaction suspension wasconcentrated under reduced pressure, hexane (100 ml) was added to theresidue and the mixture was concentrated twice under reduced pressure.To the residue was added a mixed solution (100 ml) of diethylether/hexane=1/2 and the mixture was stirred for 30 min. The solid wascollected by filtration to give the title compound (4.88 g, 96%).

¹H-NMR (DMSO-D₆) δ: 0.93 (t, 3H, J=7.5 Hz), 1.34-1.44 (m, 2H), 1.71-1.80(m, 2H), 3.10 (t, 2H, J=7.5 Hz), 4.21 (d, 2H, J=5.6 Hz), 6.86 (s, 1H),8.57 (s, 1H), 9.83 (t, 1H, J=5.6 Hz).

Example 4 Production of[(5,6-diethyl-7-hydroxy[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid hydrochloride Step 4-1

Under a nitrogen stream, the compound (3.98 g) obtained in the samemanner as in step 1-6 and tetrahydrofuran (40 ml) were mixed, and asolution of iodine (3.4 g) in tetrahydrofuran (16 ml) was added dropwiseunder cooling with dry ice/denatured ethanol. To this mixture was addeddropwise 1M lithium bis(trimethylsilyl)amide (26.8 ml) over 10 min.After stirring as is for 2.5 hr, the reaction mixture was poured into amixture of saturated aqueous ammonium chloride solution (40 ml) andwater (40 ml) under ice-cooling. To this mixture was added sodiumsulfite (1.7 g), and the organic layer was separated from the mixture.The organic layer was concentrated under reduced pressure, the obtainedresidue was combined with the aqueous layer, and the mixture wasextracted twice with ethyl acetate. The organic layer was washed withsaturated brine (70 ml), dried over sodium sulfate, sodium sulfate wasfiltered off, and the filtrate was concentrated under reduced pressure.The obtained residue was purified by column chromatography. The obtainedpurification product was recrystallized from heptane/chloroform to givethe compound described in the above-mentioned scheme (0.295 g, 4%).

¹H-NMR (CDCl₃) δ: 1.38 (t, 3H, J=7.1 Hz), 4.50 (q, 2H, J=7.1 Hz), 5.22(s, 2H), 7.36-7.56 (m, 5H), 8.33 (s, 1H).

Step 4-2

In the same manner as in Example 1, step 1-8, the compound described inthe above-mentioned scheme (0.019 g, 30%) was obtained from the compound(0.1 g) obtained in step 4-1.

¹H-NMR (CDCl₃) δ: 1.38 (t, 3H, J=7.1 Hz), 4.50 (q, 2H, J=7.1 Hz), 5.09(s, 2H), 5.73 (dd, 1H, J=17.7, 1.4 Hz), 5.76 (dd, 1H, J=11.5, 1.4 Hz),6.05 (dd, 1H, J=11.5, 1.4 Hz), 6.77 (dd, 1H, J=17.7, 11.7 Hz), 6.87 (dd,1H, J=17.7, 1.2 Hz), 7.14 (dd, 1H, J=17.7, 11.5 Hz), 7.35-7.44 (m, 5H),8.37 (s, 1H).

Step 4-3

In the same manner as in Example 2, step 2-5, the compound described inthe above-mentioned scheme (0.020 g, 75%) was obtained from the compound(0.036 g) obtained in step 4-2.

¹H-NMR (CDCl₃) δ: 1.23 (t, 3H, J=7.5 Hz), 1.36 (t, 3H, J=7.5 Hz), 1.52(t, 3H, J=7.3 Hz), 2.78 (q, 2H, J=7.5 Hz), 3.25 (q, 2H, J=7.5 Hz), 4.64(q, 2H, J=7.3 Hz), 8.26 (s, 1H), 13.10 (s, 1H)

Step 4-4

The compound (0.020 g) obtained in step 4-3 and 2-methoxyethanol (2 ml)were mixed, and glycine sodium salt (0.030 g) was added. After stirringat 130° C. for 1.5 hr, the mixture was cooled to room temperature. 1NHydrochloric acid (0.34 ml) and water (10 ml) were added to the reactionmixture and the mixture was stirred. The precipitate was collected byfiltration and dried under reduced pressure. To the obtained solid wereadded ethyl acetate (1 ml) and 4N hydrochloric acid-ethyl acetate (0.1ml) and the mixture was stirred at room temperature for 20 min. Thesolid was collected by filtration to give the title compound (0.052 mg,67%).

¹H-NMR (DMSO-D6) δ: 1.15 (t, 3H, J=7.5 Hz), 1.29 (t, 3H, J=7.5 Hz), 2.72(q, 2H, J=7.5 Hz), 3.20 (q, 2H, J=7.6 Hz), 4.21 (d, 2H, J=5.6 Hz), 8.52(s, 1H), 9.95 (t, 1H, J=5.6 Hz).

Example 5 Production of[(7-hydroxy-6-phenethyl[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid hydrochloride Step 5-1

The compound (1.31 g) obtained by a method similar to Example 4, step4-1, tetrakis(triphenylphosphine)palladium(0) (0.137 g) andtetrahydrofuran (15 ml) were mixed, and tri-n-butyltin hydride (0.7 ml)was added under ice-cooling. After stirring under ice-cooling for 20min, the mixture was stirred at room temperature for 20 min, andconcentrated under reduced pressure. The obtained residue was purifiedby column chromatography (eluent: hexane/ethyl acetate=10/0-1/1) to givethe compound described in the above-mentioned scheme (0.44 g, 44%).

¹H-NMR (CDCl₃) δ: 1.39 (t, 3H, J=7.2 Hz), 4.51 (q, 2H, J=7.2 Hz), 5.23(s, 2H), 7.36-7.56 (m, 5H), 8.31 (s, 1H), 8.99 (s, 1H).

Step 5-2

In the same manner as in Example 1, step 1-8, the compound described inthe above-mentioned scheme (0.078 g, 109%) was obtained from thecompound (0.070 g) obtained in step 5-1.

¹H-NMR (CDCl₃) δ: 1.43 (t, 3H, J=7.1 Hz), 4.54 (q, 2H, J=7.1 Hz), 5.17(s, 2H), 7.13 (d, 1H, J=9.3 Hz), 7.29-7.45 (m, 11H), 8.34 (s, 1H), 8.80(s, 1H).

Step 5-3

In the same manner as in Example 2, step 2-5, the compound described inthe above-mentioned scheme (0.037 g, 72%) was obtained from the compound(0.070 g) obtained in step 5-2.

¹H-NMR (CDCl₃) δ: 1.54 (t, 3H, J=7.2 Hz), 3.00 (s, 4H), 4.66 (q, 2H,J=7.2 Hz), 7.16-7.31 (m, 5H), 8.20 (s, 1H), 8.23 (s, ¹H), 13.17 (s, 1H).

The compound obtained in this step was converted to hydrochloride in thesame manner as in Example 4, step 4-4 and according to a conventionalmethod to give the title compound.

1H-NMR (DMSO-D6) δ: 2.93 (s, 4H), 4.22 (d, 2H, J=5.7 Hz), 7.19 (tt, 1H,J=7.1, 1.8 Hz), 7.23-7.31 (m, 4H), 8.50 (s, 1H), 8.78 (s, 1H), 9.97 (s,1H).

Example 6 Production of[(5-butyl-6-chloro-7-hydroxy[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid hydrochloride Step 6-1

The compound (200 mg) obtained by a method similar to Example 4, step4-1, hexachloroethane (224 mg) and tetrahydrofuran (4.0 ml) were mixed,and lithium bis(trimethylsilyl)amide (0.473 ml) was added at −78° C.After stirring at −78° C. for 2 hr, the mixture was slowly warmed to−40° C. Thereafter, the mixture was added dropwise to saturated aqueoussodium hydrogen carbonate solution, and ethyl acetate was added. Theorganic layer was separated from the mixture, and the aqueous layer wasextracted twice with ethyl acetate. The organic layers were combined,washed twice with saturated brine, dried over sodium sulfate, andconcentrated under reduced pressure. The concentrated residue waspurified by column chromatography (eluent: hexane/ethyl acetate=3/1-2/1)to give a crude product (180 mg) containing the compound described inthe above-mentioned scheme as a main component.

Step 6-2

In the same manner as in Example 3, step 3-1, the compound described inthe above-mentioned scheme (71 mg) was obtained from the compound (180mg) obtained in step 6-1.

¹H-NMR (DMSO-D₆) δ: 0.94 (3H, t, J=7.5 Hz), 1.28 (3H, t, J=7.1 Hz),1.37-1.47 (2H, m), 1.68-1.75 (2H, m), 3.32-3.37 (2H, m), 4.37 (2H, q,J=7.1 Hz), 5.19 (2H, s), 7.37-7.52 (5H, m), 8.57 (1H, s).

Step 6-3

The compound (70 mg) obtained in step 6-2 and trifluoroacetic acid (1ml) were mixed, and the mixture was stirred at room temperature for 3hr. To this reaction mixture was added chloroform and the mixture wasconcentrated under reduced pressure. To the concentrated residue wasadded 4N hydrochloric acid-ethyl acetate (1 ml) and the mixture wasstirred. Hexane (3 ml) was added and the mixture was stirred. The solidwas collected by filtration to give the compound described in theabove-mentioned scheme (50 mg, 83%).

¹H-NMR (DMSO-D₆) δ: 0.92 (3H, t, J=7.3 Hz), 1.31 (3H, t, J=7.1 Hz),1.37-1.45 (2H, m), 1.62-1.69 (2H, m), 3.17 (2H, t, J=7.7 Hz), 4.35 (2H,q, J=7.1 Hz), 8.69 (1H, s).

Step 6-4

In the same manner as in Example 4, step 4-4, the compound described inthe above-mentioned scheme (48 mg, 88%) was obtained from the compound(50 mg) obtained in step 6-3.

1H-NMR (DMSO-D₆) δ: 0.93 (t, 3H, J=7.3 Hz), 1.36-1.47 (m, 2H), 1.64-1.72(m, 2H), 3.15-3.28 (m, 2H), 4.15 (d, 2H, J=2.8 Hz), 8.74 (br s, 1H),10.20 (br s, 1H).

Example 7 Production of[(7-hydroxy-2-methyl-5-phenethyl[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid hydrochloride Step 7-1

2,4,6-Trichloropyridine (50 g) and N,N-dimethylformamide (400 ml) weremixed, and sodium hydride (60% oil suspension) (11.5 g) was added byportions under ice-cooling. To this mixture was added dropwise underice-cooling benzyl alcohol (28 ml) over 40 min, and the mixture wasstirred at the same temperature for 3 hr. Water (550 ml) was addeddropwise under ice-cooling and the resulting solid was collected byfiltration to give the compound described in the above-mentioned scheme(50 g, 72%).

¹H-NMR (CDCl₃) δ: 5.11 (s, 2H), 6.86 (s, 2H), 7.36-7.46 (m, 5H).

Step 7-2

Under cooling in a dry ice/acetone bath, tetrahydrofuran (250 ml) andn-butyllithium (1.65M, 119 ml) were mixed, a solution of the compound(50 g) obtained in step 7-1 in tetrahydrofuran (110 ml) was addeddropwise over 30 min. To this mixture was added dropwise a solution ofdi-tert-butyl-dicarbonate (45 ml) in tetrahydrofuran (100 ml) over 1 hr,and the mixture was stirred at the same temperature for 30 min. Water(450 ml) was added to quench the reaction, ethyl acetate (200 ml) wasadded to separate the organic layer and the organic layer was washedwith water (200 ml) and saturated brine (200 ml). The organic layer wasconcentrated under reduced pressure and the residue was purified bycolumn chromatography (eluent: hexane/ethyl acetate=50/0-11/1) and theobtained solid was further slurried in hexane (100 ml) to give thecompound described in the above-mentioned scheme (15.7 g, 31%).

¹H-NMR (CDCl₃) δ: 1.53 (s, 9H), 5.11 (s, 2H), 6.86 (s, 1H), 7.32-7.46(m, 5H).

Step 7-3

The compound (15 g) obtained in step 7-2 and 1,4-dioxane (150 ml) weremixed, potassium carbonate (18 g), phenylvinylboric acid (7.1 g),[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloridedichloromethane complex (1:1) (1.8 g) and water (45 ml) were added andthe mixture was stirred at 80° C. for 1.5 hr with heating.Phenylvinylboric acid (0.64 g) was added and the mixture was stirred for1.5 hr. The mixture was cooled to room temperature, and water, ethylacetate and saturated brine were added to separate the organic layer.The organic layer was concentrated under reduced pressure and theobtained residue was purified by column chromatography (eluent:chloroform). To the obtained solid was added isopropyl alcohol (100 ml)and the mixture was slurried at 70° C. for 0.5 hr and under ice-coolingto give the compound described in the above-mentioned scheme (11.5 g,62%).

¹H-NMR (CDCl₃) δ: 1.55 (s, 9H), 5.21 (s, 2H), 6.87 (s, 1H), 7.01 (d, 1H,J=15.9 Hz), 7.30-7.44 (m, 8H), 7.56 (d, 2H, J=7.1 Hz), 7.65 (d, 1H,J=16.1 Hz).

Step 7-4

The compound (11.5 g) obtained in step 7-3, ethyl acetate (120 ml) and2% platinum-carbon (2.5 g) were mixed, and the mixture was stirred undera hydrogen atmosphere (3.8 kgf/cm²) at room temperature for 23 hr. Thereaction mixture was filtered through celite, and the filtrate wasconcentrated under reduced pressure to give the compound described inthe above-mentioned scheme (11.5 g, 100%).

¹H-NMR (CDCl₃) δ: 1.55 (s, 9H), 3.02 (br s, 4H), 5.05 (s, 2H), 6.55 (s,1H), 7.16-7.41 (m, 10H).

Step 7-5

In the same manner as in Example 1, step 1-4, the compound described inthe above-mentioned scheme (11.9 g, 104%) was obtained from the compound(11.5 g) obtained in step 7-4.

¹H-NMR (CDCl₃) δ: 1.39 (s, 9H), 2.92 (t, 2H, J=8.2 Hz), 3.03 (t, 2H,J=8.2 Hz), 4.05 (br s, 2H), 5.00 (s, 2H), 6.10 (s, 1H), 7.16-7.43 (m,10H), 8.10 (s, 1H).

Step 7-6

The compound (126 mg) obtained in step 7-5, p-toluenesulfonic acidmonohydrate (50 mg) and trimethyl orthoformate (1 ml) were mixed,toluene (1 ml) was added and the mixture was heated at 60° C. for 1 hr.The reaction mixture was added dropwise at room temperature to saturatedaqueous sodium hydrogen carbonate solution, and ethyl acetate was addedto separate the organic layer. The organic layer was concentrated underreduced pressure and the concentrated residue was purified by thin layerchromatography (eluent: chloroform/methanol=9:1) to give the compounddescribed in the above-mentioned scheme (32 mg, 24%).

¹H-NMR (CD₃OD) δ: 1.51 (9H, s), 2.93 (3H, s), 3.06 (2H, t, J=7.6 Hz),3.52 (2H, t, J=7.6 Hz), 5.16 (2H, s), 6.72 (1H, s), 7.14-7.48 (10H, m).

Step 7-7

In the same manner as in Example 1, step 1-6, the compound described inthe above-mentioned scheme (29 mg, 53%) was obtained from the compound(55 mg) obtained in step 7-6.

¹H-NMR (CD₃OD) δ: 1.49 (9H, s), 2.52 (3H, s), 3.13 (2H, t, J=7.6 Hz),3.42 (2H, t, J=7.7 Hz), 5.16 (2H, s), 6.83 (1H, s), 7.15-7.19 (3H, m),7.24-7.28 (2H, m), 7.32-7.44 (5H, m).

Step 7-8

The compound (54 mg) obtained in step 7-7 and chloroform (0.5 ml) weremixed, trifluoroacetic acid (0.22 ml) was added, and the mixture wasstirred at room temperature for 2 hr. The reaction mixture wasconcentrated under reduced pressure, and the residue was azeotropicallydistilled with toluene to give a crude product (69 mg) containing thecompound described in the above-mentioned scheme as a main component.

The compound obtained in this step was treated in the same manner as inExample 1, step 1-10 to step 1-12, and the obtained compound wasconverted to hydrochloride by a conventional method to give the titlecompound.

¹H-NMR (DMSO-D6) δ: 2.52 (s, 3H), 3.10 (t, 2H, J=7.8 Hz), 3.35 (t, 2H,J=7.8 Hz), 4.19 (d, 2H, J=5.7 Hz), 6.69 (s, ¹H), 7.18-7.31 (m, 5H), 9.81(t, 1H, J=5.5 Hz).

Example 8 Production of{[8-(3,3-dimethyl-butyl)-6-hydroxy[1,2,4]triazolo[1,5-a]pyridine-5-carbonyl]amino}aceticacid hydrochloride Step 8-1

2-Amino-3,5-dibromopyridine (50.4 g), 2,5-hexanedione (23.5 g) andp-toluenesulfonic acid monohydrate (2.7 g) were dissolved in toluene(300 ml), and the mixture was heated under reflux for 5 hr whileremoving water. The mixture was allowed to cool to room temperature,ethyl acetate was added, and the mixture was washed successively withsaturated aqueous sodium hydrogen carbonate solution, water andsaturated brine (once each). The organic layer was dried over sodiumsulfate, filtered, and concentrated under reduced pressure to give acrude product (66.6 g) of the compound described in the above-mentionedscheme.

¹H-NMR (CDCl₃) δ: 2.00 (6H, s), 5.92 (2H, s), 8.22 (1H, d, J=2.4 Hz),8.63 (1H, d, J=2.4 Hz).

Step 8-2

In the same manner as in Example 1, step 1-3, the compound described inthe above-mentioned scheme (58.4 g, 82%) was obtained from the compound(66.6 g) obtained in step 8-1.

¹H-NMR (CDCl₃) δ: 1.99 (6H, s), 5.15 (2H, s), 5.89 (2H, s), 7.37-7.48(5H, m), 7.64 (1H, d, J=2.8 Hz), 8.31 (1H, d, J=2.8 Hz).

Step 8-3

The compound (58.4 g) obtained in step 8-2, hydroxylammonium chloride(233 g), ethanol (600 ml) and water (350 ml) were mixed. To this mixturewas added dropwise at room temperature triethylamine (46 ml), ethanol(100 ml) was added and the mixture was heated under reflux at a bathtemperature of 95° C. for 89 hr. The reaction mixture was ice-cooled,and 50% aqueous sodium hydroxide solution (96 ml), 8N aqueous sodiumhydroxide solution (134 ml) and saturated aqueous sodium hydrogencarbonate solution (50 ml) were successively added. Water (1800 ml) wasadded at room temperature, the mixture was stirred for 1 hr and aprecipitated solid was collected by filtration. The precipitated solidwas dried under reduced pressure overnight and the crude product (49 g)was slurried in 2-propanol (120 ml) to give the compound described inthe above-mentioned scheme (34.3 g, 75%).

¹H-NMR (CDCl₃) δ: 4.60 (2H, br s), 5.00 (2H, s), 7.31-7.40 (5H, m), 7.41(1H, d, J=2.8 Hz), 7.83 (1H, d, J=2.8 Hz).

Step 8-4

The compound (7.25 g) obtained in step 8-3, N,N-dimethylformamide (11ml) and N,N-dimethylformamide dimethyl acetal (11 ml) were mixed, andthe mixture was stirred with heating at 130° C. for 15 min. Afterstirring at room temperature for 20 min, the mixture was concentratedunder reduced pressure. To the obtained residue were added methanol (58ml) and pyridine (4.2 ml), and hydroxylamine-O-sulfonic acid (4.1 g) wasadded to the mixture under ice-cooling. After stirring at roomtemperature overnight, water (29 ml) and saturated aqueous sodiumhydrogen carbonate solution (58 ml) were added under ice-cooling, andthe mixture was stirred at room temperature for 1 hr. The resultingsolid was collected by filtration to give the compound described in theabove-mentioned scheme (6.13 g, 78%).

¹H-NMR (CDCl₃) δ: 5.09 (s, 2H), 7.36-7.45 (m, 5H), 7.66 (d, 1H, J=2.0Hz), 8.19 (d, 1H, J=2.0 Hz), 8.29 (s, 1H).

Step 8-5

In the same manner as in Example 1, step 1-1, the compound described inthe above-mentioned scheme (5.67 g, 49%) was obtained from the compound(10 g) obtained in step 8-4.

¹H-NMR (DMSO-D₆) δ: 5.33 (s, 2H), 7.31-7.49 (m, 5H), 8.37 (s, 1H), 8.56(s, 1H).

Step 8-6

To the compound (5.68 g) obtained in step 8-5 was added toluene (57 ml),and N,N-dimethylformamide diethyl acetal (4.5 ml) was added in 3portions at 80° C. After completion of the reaction, the mixture wasconcentrated under reduced pressure, and the obtained residue waspurified by column chromatography (eluent: chloroform/ethylacetate=10/1-4/1). Hexane was added to the obtained compound, and theprecipitated solid was slurried to give the compound described in theabove-mentioned scheme (4.68 g, 69%).

¹H-NMR (CDCl₃) δ: 1.39 (t, 3H, J=7.1 Hz), 4.53 (q, 2H, J=7.1 Hz), 5.21(s, 2H), 7.35-7.43 (m, 5H), 7.72 (s, 1H), 8.38 (s, 1H).

Step 8-7

The compound (100 mg) obtained in step 8-6, tert-butylacetylene (0.1ml), bis(triphenylphosphine)palladium(II) dichloride (18 mg), and copperiodide(I) (5 mg) were added to a screw bottle. To this mixture wereadded tetrahydrofuran (0.4 ml) and triethylamine (0.8 ml) and the bottlewas tightly sealed. The mixture was stirred at room temperature for 1hr, passed though a small amount of silica gel and concentrated underreduced pressure. The residue was purified twice by thin layerchromatography (eluent: hexane/ethyl acetate=2/1) to give the compounddescribed in the above-mentioned scheme (85 mg, 85%).

Step 8-8

In the same manner as in Example 2, step 2-5, the compound described inthe above-mentioned scheme (62 mg, 94%) was obtained from the compound(85 mg) obtained in step 8-7.

In the same manner as in Example 4, step 4-4, the title compound wasobtained from the compound obtained in this step.

¹H-NMR δ: 0.98 (s, 9H), 1.57-1.66 (m, 2H), 2.89-2.99 (m, 2H), 4.25 (d,2H, J=5.4 Hz), 7.42 (s, 1H), 8.64 (s, 1H), 10.42 (t, 1H, J=5.4 Hz),13.28 (s, 1H).

Example 9 Production of[(7-hydroxy-6-phenyl[1,2,4]triazolo[4,3-a]pyridine-8-carbonyl)amino]aceticacid Step 9-1

The hydroxyl-protecting group of the compound obtained in Example 1,step 1-3 was removed in the same manner as in Example 2, step 2-5. To asolution of the obtained compound (3.30 g) in chloroform (30 ml) wasadded under ice-cooling N-bromosuccinimide (2.82 g). After stirring atroom temperature for 5 hr, the reaction mixture was separated by addingsaturated aqueous sodium hydrogen carbonate solution (20 ml). Theorganic layer was further washed with aqueous sodium sulfite solutionand saturated brine, and dried over anhydrous magnesium sulfate. Afterfiltration, the mixture was concentrated under reduced pressure to givethe compound described in the above-mentioned scheme (5.37 g) as a crudeproduct.

¹H-NMR (CDCl₃) δ: 1.66 (9H, s), 8.39 (1H, s), 12.77 (1H, s).

Step 9-2

To a solution of the compound (5.37 g) obtained in step 9-1 inN,N-dimethylformamide were added under ice-cooling potassium carbonate(2.19 g) and benzyl bromide (1.88 ml) and the mixture was stirred atroom temperature for 20 hr. The reaction mixture was separated by addingwater (50 ml) and ethyl acetate (50 ml). The organic layer was furtherwashed with saturated brine, dried over anhydrous magnesium sulfate, andconcentrated under reduced pressure. The residue was purified by columnchromatography (eluent: hexane/ethyl acetate=3/1-1/2) to give thecompound described in the above-mentioned scheme (3.73 g, 2 steps 65%).

¹H-NMR (CDCl₃) δ: 1.58 (9H, s), 5.21 (2H, s), 7.19-7.21 (2H, m),7.37-7.46 (3H, m), 7.76 (1H, s).

Step 9-3

To the compound (610 mg) obtained in step 9-2 was added trifluoroaceticacid (180 ml) under ice-cooling, and the mixture was stirred at roomtemperature for 2 hr. The reaction mixture was diluted with chloroform(6 ml) and concentrated under reduced pressure. Chloroform (6 ml) wasadded again to the residue, thionyl chloride (0.18 ml) andN,N-dimethylformamide (one drop) were added, and the mixture was heatedat 70° C. for 30 min. The obtained solution was concentrated underreduced pressure to give the compound described in the above-mentionedscheme (540 mg, 98%).

Step 9-4

To a solution of the compound (540 mg) obtained in step 9-3 intetrahydrofuran (6 ml) were added under ice-coolingdiisopropylethylamine (0.29 ml) and glycine tert-butyl ester (0.21 ml),and the mixture was stirred for 2 hr. To the reaction mixture were addeddiisopropylethylamine (0.29 ml) and tert-butyl carbazate, and themixture was heated at 70° C. for 3 hr. The reaction mixture wasconcentrated under reduced pressure, and the residue was purified bycolumn chromatography (eluent: hexane/ethyl acetate=3/1-3/2) to give thecompound described in the above-mentioned scheme (790 mg, 92%).

¹H-NMR (CDCl₃) δ: 1.30 (9H, s), 1.48 (9H, s), 4.05 (2H, d, J=5.5 Hz),5.24 (2H, s), 6.27 (1H, s), 7.14 (2H, t, J=4.1 Hz), 7.34-7.41 (3H, m),7.47 (1H, s), 11.50 (1H, t, J=5.4 Hz), 11.83 (1H, s).

Step 9-5

In the same manner as in Example 1, step 1-8, the compound described inthe above-mentioned scheme (280 g, 84%) was obtained from the compound(330 mg) obtained in step 9-4.

¹H-NMR (CDCl₃) δ: 1.31 (9H, s), 1.48 (9H, s), 4.06 (2H, d, J=5.5 Hz),5.30 (2H, s), 6.16 (1H, s), 7.17 (2H, d, J=7.4 Hz), 7.18 (1H, s),7.28-7.40 (6H, m), 7.43-7.46 (2H, m), 11.79 (1H, s), 11.85 (1H, t, J=5.4Hz).

Step 9-6

In the same manner as in Example 2, step 2-5, the compound described inthe above-mentioned scheme (86 mg, 87%) was obtained from the compound(120 mg) obtained in step 9-5.

¹H-NMR (CDCl₃) δ: 1.45 (9H, s), 1.49 (9H, s), 4.15 (2H, s), 7.06-7.29(8H, m), 10.40 (1H, s), 10.95 (1H, s).

Step 9-7

To a solution of the compound (110 mg) obtained in step 9-6 inchloroform (0.3 ml) was added 4N hydrochloric acid dioxane solution (1ml), and the mixture was stirred under ice-cooling for 2 hr. Thereaction mixture was concentrated under reduced pressure to give thecompound described in the above-mentioned scheme (84 mg, 87%).

¹H-NMR (CD₃OD) δ: 1.49 (9H, s), 4.04 (2H, s), 7.36-7.47 (5H, m), 7.57(1H, s).

Step 9-8

To the compound (41 mg) obtained in step 9-7 was added trimethylorthoformate (0.41 ml), and the mixture was heated at 100° C. for 30min. The reaction mixture was concentrated under reduced pressure, andthe residue was dissolved in chloroform (1 ml). Trifluoroacetic acid (2ml) was added and the mixture was stirred at room temperature for 3 hr.The reaction mixture was concentrated under reduced pressure, 4Nhydrochloric acid dioxane solution (1 ml) was added, and the mixture wasstirred at room temperature for 30 min. The reaction mixture wasconcentrated under reduced pressure and the residue was slurried inwater to give the title compound (29 mg, 89%).

¹H-NMR (DMSO-D₆) δ: 4.06 (2H, d, J=5.5 Hz), 7.39-7.46 (3H, m), 7.60 (2H,dd, J=8.3, 1.4 Hz), 8.39 (1H, s), 8.86 (1H, s), 10.50 (1H, t, J=5.7 Hz),12.59 (1H, s), 13.75 (1H, s).

Example 10 Production of[(7-hydroxy[1,2,4]triazolo[4,3-a]pyridine-8-carbonyl)amino]acetic acidhydrochloride Step 10-1

In the same manner as in the deprotection reaction of thecarboxyl-protecting group in Example 9, step 9-8, a crude productcontaining the compound described in the above-mentioned scheme as amain component was obtained from the compound (0.050 g) obtained inExample 1, step 1-5.

¹H-NMR (DMSO-D₆) δ: 5.60 (s, 2H), 7.35-7.55 (m, 5H), 7.69 (d, 1H, J=7.7Hz), 9.03 (d, 1H, J=7.7 Hz), 9.48 (s, 1H).

Step 10-2

In the same manner as in Example 1, step 1-10, the compound described inthe above-mentioned scheme (0.024 g, 41%) was obtained from the compoundobtained in step 10-1.

¹H-NMR (CDCl₃) δ: 1.51 (s, 9H), 4.23 (d, 2H, J=5.6 Hz), 5.35 (s, 2H),6.81 (d, 1H, J=7.7 Hz), 7.26-7.51 (m, 5H), 8.10 (d, 1H, J=7.7 Hz), 8.67(s, 1H), 9.66 (br s, 1H).

The compound obtained in this step was subjected to removal of thehydroxyl-protecting group and carboxyl-protecting group in the samemanner as above, and the obtained compound was converted tohydrochloride by a conventional method to give the title compound.

¹H-NMR (DMSO-D₆) δ: 4.07 (s, 2H), 6.65 (d, 1H, J=7.7 Hz), 8.32 (d, 1H,J=7.7 Hz), 8.99 (s, 1H), 10.09 (s, 1H).

Example 11 Production of[(6-hydroxy[1,2,3]triazolo[1,5-a]pyridine-7-carbonyl)amino]acetic acidStep 11-1

2-Bromo-5-hydroxypyridine (5.8 g), N,N-dimethylformamide (58 ml) andpotassium carbonate (5.1 g) were mixed, benzyl bromide (4.4 ml) wasadded under ice-cooling and the mixture was stirred at room temperaturefor 13 hr. To the reaction mixture were added ethyl acetate (58 ml) andwater (87 ml) and the organic layer was separated from the mixture andwashed successively with water (60 ml, 30 ml) twice and with saturatedbrine (30 ml). The organic layer was dried over anhydrous magnesiumsulfate, and filtered. The filtrate was concentrated under reducedpressure. The obtained residue was purified by column chromatography(eluent: hexane/ethyl acetate=10/1-7/1) to give the compound describedin the above-mentioned scheme (7.4 g, 83%).

¹H-NMR (CDCl₃) δ: 5.09 (s, 2H), 7.15 (dd, 1H, J=8.1, 3.2 Hz), 7.33-7.38(m, 1H), 7.36 (d, 1H, J=8.1 Hz), 7.40-7.41 (m, 4H), 8.13 (d, 1H, J=3.2Hz).

Step 11-2

To n-butyllithium (1.54 mol/l hexane solution 25 ml) was added dropwisea solution of the compound (1 g) obtained in step 11-1 in toluene (4 ml)at −78° C. over 7 min. The reaction mixture was stirred at −78° C. for50 min, and a solution of N,N-dimethylformamide (0.352 ml) in toluene (4ml) was added dropwise. The reaction mixture was further stirred at −78°C. for 1 hr, water (6 ml) was added at −10° C., and the mixture wasstirred at room temperature for 2 hr. The organic layer and the aqueouslayer were separated, the aqueous layer was extracted twice with toluene(5 ml). The organic layers were combined and washed with saturated brine(10 ml). The organic layer was dried over anhydrous magnesium sulfate,and the mixture was filtered. The filtrate was concentrated underreduced pressure and the obtained residue was purified by columnchromatography (eluent: hexane/ethyl acetate=10/1-7/1) to give thecompound described in the above-mentioned scheme (641 mg, 79%).

¹H-NMR (CDCl₃) δ: 5.21 (s, 2H), 7.35-7.45 (m, 6H), 7.95 (d, 1H, J=8.9Hz), 8.51 (d, 1H, J=2.8 Hz), 9.99 (s, 1H).

Step 11-3

The compound (637 mg) obtained in step 11-2, methanol (6.4 ml) andtosylhydrazide (574 mg) were mixed, and the mixture was heated underreflux for 10 min. The reaction mixture was concentrated under reducedpressure, morpholine (6.4 ml) was added, and the mixture was heatedunder reflux for 30 min. The reaction mixture was concentrated underreduced pressure, and ethyl acetate (12 ml), 2M aqueous sodium carbonatesolution (6 ml) and water (5 ml) were added. Further, tetrahydrofuran (6ml) was added and the organic layer was separated. The aqueous layer wasextracted twice with ethyl acetate (5 ml), and the organic layers werecombined and washed with saturated brine (10 ml). The organic layer wasdried over anhydrous magnesium sulfate, and filtered. The filtrate wasconcentrated under reduced pressure and the obtained solid was slurriedin diisopropyl ether to give the compound described in theabove-mentioned scheme (566 mg, 84%).

¹H-NMR (CDCl₃) δ: 5.12 (s, 2H), 7.11 (dd, 1H, J=9.7, 2.0 Hz), 7.36-7.47(m, 5H), 7.61 (dd, 1H, J=9.7, 0.8 Hz), 7.99 (d, 1H, J=0.8 Hz), 8.34 (d,1H, J=2.0 Hz).

Step 11-4

The compound (200 mg) obtained in step 11-3 and tetrahydrofuran (2 ml)were mixed, and lithium diisopropylamide (2M tetrahydrofuran, heptane,ethylbenzene solution, 0.45 ml) was added at −40° C. After stirring at−40° C. for 1 hr, dry ice was added, and the mixture was allowed to warmto room temperature by stirring for 1 hr. Thereafter, methanol (2 ml)was added, and the reaction mixture was concentrated under reducedpressure to give the compound described in the above-mentioned scheme asa crude product. This was directly used for the next step.

Step 11-5

In the same manner as in Example 1, step 1-10, the compound described inthe above-mentioned scheme (85 mg, 28% (2 step)) was obtained from thecrude product obtained in step 11-4.

¹H-NMR (CDCl₃) δ: 3.80 (s, 3H), 4.38 (d, 2H, J=5.2 Hz), 5.32 (s, 2H),7.24 (d, 1H, J=9.7 Hz), 7.31-7.41 (m, 3H), 7.46-7.49 (m, 2H), 7.75 (d,1H, J=9.7 Hz), 8.11 (s, 1H), 8.79 (br s, 1H).

Step 11-6

In the same manner as in Example 2, step 2-5, the compound described inthe above-mentioned scheme (40 mg, 76%) was obtained from the compound(72 mg) obtained in step 11-5.

¹H-NMR (CDCl₃) δ: 3.83 (s, 3H), 4.37 (d, 2H, J=6.0 Hz), 7.17 (d, 1H,J=9.7 Hz), 7.80 (d, 1H, J=9.7 Hz), 8.12 (s, 1H), 10.57 (br s, 1H), 13.56(s, 1H).

The compound obtained in this step was subjected to removal of thecarboxyl group in the same manner as above to give the title compound.

¹H-NMR (DMSO-D₆) δ: 4.28 (d, 2H, J=5.2 Hz), 7.31 (d, 1H, J=9.7 Hz), 8.20(d, 1H, J=9.7 Hz), 8.39 (s, 1H), 10.36 (t, 1H, J=5.2 Hz), 13.82 (s, 1H).

Example 116 Production of[(7-hydroxy-5-phenethyl[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid Step 116-1

Cyanamide (1.4 g) and 1,4-dioxane (20 ml) were mixed, and dimethyl1,3-acetonedicarboxylate (2.0 g) and nickel(II) acetylacetonate (0.30 g)were added. The mixture was heated under reflux for 16 hr. The mixturewas cooled to room temperature, stirred for 1 hr and the resulting solidwas collected by filtration. To the obtained solid was added methanol(6.0 ml) and the mixture was stirred at room temperature for 1.5 hr. Thesolid was collected by filtration to give the compound described in theabove-mentioned scheme (1.4 g, 64%).

¹H-NMR (DMSO-D₆) δ: 3.80 (s, 3H), 4.92 (s, 1H), 7.20 (s, 2H), 10.29 (s,1H), 11.51 (s, 1H).

Step 116-2

The compound (30 g) obtained in step 116-1, phosphorus oxychloride (150ml) and N,N-diisopropylethylamine (30 ml) were mixed, and the mixturewas stirred at room temperature for 3 days. The reaction mixture wasconcentrated, and azeotropically distilled 3 times with toluene. Underice-cooling, methanol (30 ml) and water (150 ml) were added and themixture was stirred at room temperature for 1 hr. The resulting solidwas collected by filtration, and combined with the solid resulting fromthe filtrate. Methanol (50 ml) was added and the mixture was stirred atroom temperature for 1 hr. The solid was collected by filtration to giveprimary crystals. The filtrate was concentrated, and methanol (10 ml)was added to the residue, and the resulting solid was collected byfiltration to give a secondary crystal. The primary crystal and thesecondary crystal were combined to give the compound described in theabove-mentioned scheme (21 g, 59%).

¹H-NMR (DMSO-D₆) δ: 3.84 (s, 3H), 6.84 (s, 1H), 7.16 (br s, 2H).

Step 116-3

The compound (2.2 g) obtained in step 116-2 and 2-propanol (31 ml) weremixed, and N,N-dimethylformamide dimethyl acetal (2.9 ml) was added. Themixture was heated under reflux for 30 min. The reaction mixture wascooled to room temperature, hydroxylamine.hydrochloride (1.4 g) wasadded, and the mixture was stirred at room temperature for 30 min. Thereaction mixture was concentrated to an about half amount, and water (40ml) and 2-propanol (6.6 ml) were added. The mixture was stirred at roomtemperature for 30 min, and the resulting solid was collected byfiltration to give the compound described in the above-mentioned scheme(2.2 g, 84%).

¹H-NMR (DMSO-D₆) δ: 3.92 (s, 3H), 7.37 (s, 1H), 7.85 (d, 1H, J=9.5 Hz),10.12 (d, 1H, J=9.5 Hz), 10.83 (s, 1H).

Step 116-4

The compound (0.66 g) obtained in step 116-3 and tetrahydrofuran (6.6ml) were mixed, and trifluoroacetic anhydride (0.37 ml) was added. Themixture was heated under reflux for 22 hr. The reaction mixture wascooled to room temperature, ethyl acetate and saturated aqueous sodiumhydrogen carbonate solution were added, and the organic layer wasseparated. The organic layer was washed with saturated brine, and driedover sodium sulfate. After filtration, the filtrate was concentratedunder reduced pressure and the obtained residue was purified by columnchromatography (eluent: chloroform/ethyl acetate=4/1) to give thecompound described in the above-mentioned scheme (0.32 g, 51%).

¹H-NMR (DMSO-D₆) δ: 3.99 (s, 3H), 7.92 (s, 1H), 8.71 (s, 1H).

Step 116-5

The compound (1.0 g) obtained in step 116-4, phenethylboronic acid (1.2g), potassium carbonate (1.7 g),[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloridedichloromethane complex (1:1) (0.083 g), cyclopentyl methyl ether (6.0ml) and water (0.15 ml) were mixed, and the mixture was stirred withheating at 50° C. for 6 hr. The reaction mixture was cooled to roomtemperature, and the organic layer was washed twice with 3% aqueousdiethylenetriamine solution (10 ml) and saturated brine (5 ml). Sodiumsulfate and metal scavenger silica gel (1 g) were added and the mixturewas stirred at room temperature for 1 hr, and filtered through aKiriyama funnel packed with silica gel (1 g). The filtrate wasconcentrated under reduced pressure to give the compound described inthe above-mentioned scheme (1.87 g) as a crudely purified product.

¹H-NMR (CDCl₃) δ: 3.17 (t, 2H, J=7.8 Hz), 3.48 (t, 2H, J=7.8 Hz), 4.08(s, 3H), 6.84 (s, 1H), 7.18-7.28 (m, 5H), 8.42 (s, 1H).

Step 116-6

The compound (1.87 g) obtained in step 116-5 and tetrahydrofuran weremixed, and 4N aqueous sodium hydroxide solution (4.0 ml) was added underice-cooling. After stirring at room temperature for 2 hr, the reactionmixture was neutralized with concentrated hydrochloric acid (1.4 ml)under ice-cooling. To the suspension were added ethanol (5 ml) and water(1.3 ml) and the mixture was stirred for 1 hr. The solid was collectedby filtration to give the compound described in the above-mentionedscheme (0.847 g, 69%).

¹H-NMR (DMSO-D₆) δ: 3.13 (t, 2H, J=7.8 Hz), 3.45 (t, 2H, J=7.8 Hz),7.23-7.31 (m, 5H), 8.65 (s, 1H), 14.19 (s, 1H).

Step 116-7

The compound (0.200 g) obtained in step 116-6, acetonitrile (1.0 ml),1-hydroxybenzotriazole monohydrate (0.122 g) and glycine methyl esterhydrochloride (0.100 g) were mixed, and triethylamine (0.111 ml) and1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.153 g)were added under ice-cooling. The mixture was stirred at roomtemperature for 2 hr. Saturated aqueous sodium hydrogen carbonatesolution (2 ml) was added to the reaction mixture and the precipitatedsolid was collected by filtration to give the compound described in theabove-mentioned scheme (0.194 g, 78%).

¹H-NMR (CDCl₃) δ: 3.18 (t, 2H, J=7.8 Hz), 3.48 (t, 2H, J=7.8 Hz), 3.81(s, 3H), 4.34 (d, 2H, J=5.2 Hz), 6.92 (s, 1H), 7.15-7.33 (m, 5H), 8.42(s, 1H), 9.90 (s, 1H).

Step 116-8

The compound (0.150 g) obtained in step 116-7, 2-ethoxyethanol (0.75 ml)and 8N aqueous sodium hydroxide solution (0.23 ml) were mixed and themixture was stirred at 90° C. for 18 hr. To this mixture were addedethanol (0.75 ml) and water (0.23 ml) and the mixture was stirred atroom temperature for 1 hr. The solid was collected by filtration to givea crudely purified product of the compound described in theabove-mentioned scheme (0.19 g).

¹H-NMR (DMSO-D₆) δ: 2.99-3.11 (m, 4H), 3.58 (d, 2H, J=4.4 Hz), 6.01 (s,1H), 7.20-7.27 (m, 5H), 7.86 (s, 1H), 11.23 (t, 1H, J=4.4 Hz).

Step 116-9

The compound (0.19 g) obtained in step 116-8 and water (0.63 ml) weremixed and the mixture was warmed to 50° C. Acetone (0.78 ml) and 6Nhydrochloric acid (0.2 ml) were added, and the mixture was stirred atthe same temperature for 1 hr. After stirring under ice-cooling for 1hr, the solid was collected by filtration to give the compound describedin the above-mentioned scheme (0.11 g, 80%).

¹H-NMR (DMSO-D₆) δ: 3.12 (t, 2H, J=7.9 Hz), 3.40 (t, 3H, J=7.9 Hz), 4.22(d, 2H, J=5.2 Hz), 6.79 (s, 1H), 7.21-7.29 (m, 5H), 8.58 (s, 1H), 9.84(t, 1H, J=5.2 Hz), 12.97 (s, 1H), 14.22 (s, 1H).

Step 116-10

The compound (0.050 g) obtained in step 116-9 and methanol (3 ml) weremixed and the mixture was heated to 60° C. The solution was cooled toroom temperature and stirred for one day. The solid was collected byfiltration to give the title compound (0.031 g, 61%).

¹H-NMR (DMSO-D₆) δ: 3.12 (t, 2H, J=7.9 Hz), 3.40 (t, 3H, J=7.9 Hz), 4.22(d, 2H, J=5.2 Hz), 6.79 (s, 1H), 7.21-7.29 (m, 5H), 8.58 (s, 1H), 9.84(t, 1H, J=5.2 Hz), 12.97 (s, 1H), 14.22 (s, 1H).

Example 117 Production of[(5-butyl-7-hydroxy[1,2,4]triazolo[1,5-a]pyridine-8-carbonyl)amino]aceticacid Step 117-1

The compound (0.050 g) obtained in step 116-4, butylboronic acid (0.042g), silver(I) oxide (0.071 g), potassium carbonate (0.084 g),[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloridedichloromethane complex (1:1) (0.008 g) and tetrahydrofuran (1.0 ml)were mixed, and the mixture was heated under reflux for 10 hr. Insolublematerial was filtered off through celite, and saturated aqueous sodiumhydrogen carbonate solution and ethyl acetate were added. The organiclayer was separated from the mixture. The organic layer was washed twicewith saturated aqueous sodium hydrogen carbonate solution and saturatedbrine, dried over sodium sulfate and filtered. The filtrate wasconcentrated under reduced pressure and the obtained residue waspurified by thin layer chromatography (eluent: hexane/ethyl acetate=1/1)to give the compound described in the above-mentioned scheme (0.046 g,77%).

¹H-NMR (CDCl₃) δ: 1.00 (t, 3H, J=7.4 Hz), 1.45-1.53 (m, 2H), 1.79-1.87(m, 2H), 3.18 (t, 2H, J=7.9 Hz), 4.08 (s, 3H), 6.92 (s, 1H), 8.38 (s,1H).

Step 117-2

The compound (0.043 g) obtained in step 117-1 and methanol (0.22 ml)were mixed, and 28% sodium methoxide methanol solution (0.014 ml) wasadded. The mixture was stirred at room temperature for 4 hr. Water (0.22ml) was added, and the mixture was stirred at room temperature for 1 hr.1N Hydrochloric acid (0.16 ml) was added to the reaction mixture, andthe resulting solid was collected by filtration to give the compounddescribed in the above-mentioned scheme (0.026 g, 66%).

¹H-NMR (CDCl₃) δ: 1.01 (t, 3H, J=7.3 Hz), 1.46-1.57 (m, 2H), 1.82-1.90(m, 2H), 3.21 (t, 2H, J=7.9 Hz), 4.15 (s, 3H), 6.77 (s, 1H), 8.28 (s,1H).

Step 117-3

The compound (0.025 g) obtained in step 117-2 and N,N-dimethylformamide(0.50 ml) were mixed, and 1-hydroxybenzotriazole monohydrate (0.016 g)and glycine tert-butylester (0.015 ml) and1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.020 g)were added. The mixture was stirred at room temperature for 1.5 hr.Under ice-cooling, 5% aqueous sodium hydrogen carbonate solution andwater were added to the reaction mixture and the resulting solid wascollected by filtration to give the compound described in theabove-mentioned scheme (0.033 g, 94%).

¹H-NMR (CDCl₃) δ: 1.00 (t, 4H, J=7.3 Hz), 1.51 (s, 9H), 1.80-1.90 (m,2H), 3.18 (t, 2H, J=7.9 Hz), 4.21 (d, 2H, J=5.2 Hz). 6.72 (s, 1H), 8.29(s, 1H), 9.72 (t, 1H, J=4.2 Hz).

Step 117-4

The compound (0.030 g) obtained in step 117-3 and 25% hydrogen bromideacetic acid solution (0.60 ml) were mixed, and the mixture was heatedunder reflux for 3 hr. The reaction mixture was concentrated underreduced pressure. To the obtained residue were added water (0.60 ml) and4N aqueous sodium hydroxide solution (0.23 ml) under ice-cooling. Then,2N hydrochloric acid (0.23 ml) was added under ice-cooling, and theresulting solid was collected by filtration to give the compounddescribed in the above-mentioned scheme (0.010 g, 42%).

¹H-NMR (DMSO-D₆) β: 0.93 (t, 3H, J=7.5 Hz), 1.33-1.44 (m, 2H), 1.71-1.80(m, 2H), 3.10 (t, 2H, J=7.5 Hz), 4.20 (d, 2H, J=5.2 Hz), 6.85 (s, 1H),8.55 (s, 1H), 9.84 (br s, 1H), 14.26 (br s, 1H).

Step 117-5

The compound (0.100 g) obtained in step 117-4 and methyl ethyl ketone(1.0 ml) were mixed, and heated to 80° C. Heptane (1.0 ml) was added tothe solution, and the mixture was stirred at room temperature overnight.The solid was collected by filtration to give the title compound (0.089g, 89%).

¹H-NMR (DMSO-D₆) δ: 0.93 (t, 3H, J=7.5 Hz), 1.33-1.44 (m, 2H), 1.71-1.80(m, 2H), 3.10 (t, 2H, J=7.5 Hz), 4.20 (d, 2H, J=5.2 Hz), 6.85 (s, 1H),8.55 (s, 1H), 9.84 (br s, 1H), 14.26 (br s, 1H).

In the same manner as in the above-mentioned Examples 1 to 11, Example116 or 117, or other conventional methods as necessary, the compounds ofExamples 12 to 115 and Examples 118 to 122 shown in the following Tables3 to 24 were produced.

The structural formulas and property data of the compounds of Examples 1to 122 are shown in the following Tables 1 to 24.

TABLE 1 Ex. MS MS No. compound name structural formula ¹H-NMR, δppm (M +H) (M − H) 1 {[5-(4-fluoro- 3- trifluoromethyl- phenyl)-7-hydroxy[1,2,4] triazolo[1,5- a]pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.31 (s, 1H),7.73-7.82 (m, 1H), 8.34- 8.43 (m, 1H), 8.43-8.51 (m, 1H), 8.61 (s, 1H),9.99 (t, 1H, J = 5.6 Hz). 399 397 2 [(7-hydroxy-5- phenethyl[1,2,4]triazolo[1,5- a]pyridine-8- carbanyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.12 (t, 2H, J = 7.8 Hz), 3.41 (t, 2H, J =7.8 Hz), 4.21 (d, 2H, J = 5.6 Hz), 6.81 (s, 1H), 7.14-7.33 (m, 5H), 8.60(s, 1H), 9.85 (t, 1H, 341 339 J = 5.6 Hz). 3 [(5-butyl-7- hydroxy[1,2,4]triazolo[1,5- a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.93 (t, 3H, J = 7.4 Hz), 1.39 (td, 2H, J =14.8, 7.4 Hz), 1.72-1.79 (m, 2H), 3.10 (t, 2H, J = 7.7 Hz), 293 291 4.21(d, 2H, J = 5.5 Hz), 6.85 (s, 1H), 8.56 (s, 1H), 9.84 (t, 1H, J = 5.6Hz). 4 [(5,6-diethyl- 7- hydroxy[1,2,4] triazolo[1,5- a]pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.15 (t, 3H, J = 7.5 Hz), 1.29 (t, 3H, J =7.5 Hz), 2.72 (q, 2H, J = 7.5 Hz), 3.20 (q, 2H, J = 7.6 Hz), 4.21 (d,2H, J = 5.6 Hz), 8.52 (s, 293 291 1H), 9.95 (t, 1H, J = 5.6 Hz). 5[(7-hydroxy-6- phenethyl[1,2,4] triazolo[1,5- a]pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.93 (s, 4H), 4.22 (d, 2H, J = 5.7 Hz),7.19 (tt, 1H, J = 7.1, 1.8 Hz), 7.23-7.31 (m, 4H), 8.50 (s, 1H), 8.78(s, 1H), 9.97 (s, 1H). 341 339

TABLE 2 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H)  6 [(5-butyl-6- chloro-7- hydroxy[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.93 (t, 3H, J = 7.3 Hz), 1.36-1.47 (m,2H), 1.64-1.72 (m, 2H), 3.15-3.28 (m, 2H), 4.15 (d, 2H, J = 2.8 Hz),8.74 (br s, 1H), 10.20 (br s, 1H). 327 325  7 [(7-hydroxy-2- methyl-5-phenethyl[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.52 (s, 3H), 3.10 (t, 2H, J = 7.8 Hz),3.35 (t, 2H, J = 7.8 Hz), 4.19 (d, 2H, J = 5.7 Hz), 6.69 (s, 1H),7.18-7.31 (m, 5H), 9.18 (t, 1H, J = 5.5 Hz). 355 353  8 {[8-(3,3-dimethylbutyl)- 6- hydroxy[1,2,4] triazolo[1,5-a] pyridine-5-carbonyl)amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.98 (s, 9H), 1.57-1.66 (m, 2H), 2.89-2.99(m, 2H), 4.25 (d, 2H, J = 5.4 Hz), 7.42 (s, 1H), 8.64 (s, 1H), 10.42 (t,1H, J = 5.4 Hz), 13.28 (s, 1H). 321 319  9 [(7-hydroxy-6- phenyl[1,2,4]triazolo[4,3-a] pyridine-8- carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.06 (d, 2H, J = 5.5 Hz), 7.39-7.46 (m,3H), 7.60 (dd, 2H, J = 8.3, 1.4 Hz), 8.39 (s, 1H), 8.86 (s, 1H), 10.50(t, 1H, J = 5.7 Hz), 12.59 (s, 1H), 13.75 (s, 1H). 313 311 10 [(7-hydroxy[1,2,4] triazolo[4,3-a] pyridine-8- carbonyl)amino] acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.07 (s, 2H), 6.65 (d, 1H, J = 7.7 Hz),8.32 (d, 1H, J = 7.7 Hz), 8.99 (s, 1H), 10.09 (s, 1H). 237 235 11 [(6-hydroxy[1,2,3] triazolo[1,5-a] pyridine-7- carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.2 Hz), 7.31 (d, 1H, J =9.7 Hz), 8.20 (d, 1H, J = 9.7 Hz), 8.39 (s, 1H), 10.36 (t, 1H, J = 5.2Hz), 13.82 (s, 1H). 237 235

TABLE 3 MS Ex. compound MS (M − No. name structural formula ¹H-NMR, δppm (M + H) H) 12 [(7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.22 (d, 2H, J = 5.6 Hz), 6.93 (d, 1H, J =7.7 Hz), 8.56 (s, 1H), 8.96 (d, 1H, J = 7.7 Hz), 9.81-9.91 (m, 1H). 237235 13 [(7-hydroxy-2- phenyl[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.27 (d, 2H, J = 5.6 Hz), 6.94 (d, 1H, J =7.7 Hz), 7.55-7.58 (m, 3H), 8.31-8.33 (m, 2H), 9.00 (d, 1H, J = 7.3 Hz),10.11 (t, 1H, J = 5.2 Hz). 313 311 14 ({5-[2-(4- chlorophenyl) ethyl]-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl}amino) acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.12 (2H, t, J = 7.9 Hz), 3.40 (2H, t, J =7.7 Hz), 4.21 (2H, d, J = 5.6 Hz), 6.80 (1H, s), 7.27 (2H, d, J = 8.5Hz), 7.35 (2H, d, J = 8.5 Hz), 8.59 (1H, s), 9.85 (1H, t, J = 5.6 Hz).375 373 15 [(2- cyclopropyl-7- hydroxy-5- phenethyl[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.04-1.12 (m, 4H), 2.17-2.23 (m, 1H), 3.10(t, 2H, J = 7.9 Hz), 3.29-3.37 (m, 2H), 4.18 (d, 2H, J = 5.3 Hz), 6.66(s, 1H), 7.18- 7.32 (m, 5H), 9.84 (t, 1H, J = 4.9 Hz), 14.10 (s, 1H).381 379 16 ({7-hydroxy-5- [2-(4- trifluoromethyl phenyl)ethyl][1,2,4]triazolo [1,5-a]pyridine- 8- carbonyl}amino) acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.21 (2H, t, J = 7.8 Hz), 3.44 (2H, t, J =7.8 Hz), 4.20 (2H, d, J = 5.8 Hz), 6.83 (1H, s), 7.48 (2H, d, J = 8.1Hz), 7.66 (2H, d, J = 8.1 Hz), 8.59 (1H, s), 9.81-9.88 (1H, m). 409 40717 ({5-[2-(4- fluorophenyl) ethyl]-7- hydroxy[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl}amino) acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.11 (2H, t, J = 7.9 Hz), 3.39 (2H, t, J =7.7 Hz), 4.21 (2H, d, J = 5.2 Hz), 6.80 (1H, s), 7.07- 7.16 (2H, m),7.23-7.30 (2H, m), 8.60 (1H, s), 9.85 (1H, t, J = 5.4 Hz). 359 357

TABLE 4 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 18 {[7-hydroxy-5- (3-methylbutyl) [1,2,4]triazolo[1,5-a]pyridine- 8-carbonyl] amino}acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.95 (6H, d, J = 6.5 Hz), 1.58-1.70 (3H,m), 3.07- 3.13 (2H, m), 4.21 (2H, d, J = 5.6 Hz), 6.87 (1H, s), 8.57(1H, s), 9.85 (1H, t, J = 5.6 Hz). 307 305 19 ({5-[2-(3,5-difluorophenyl) ethyl]-7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl}amino) acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.15 (2H, t, J = 7.8 Hz), 3.42 (2H, t, J =7.8 Hz), 4.20 (2H, d, J = 5.6 Hz), 6.83 (1H, s), 6.97- 7.11 (3H, m),8.58-8.61 (1H, m), 9.79-9.89 (1H, m). 377 375 20 [(5-cyclo-pentylmethyl- 7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.21-1.32 (2H, m), 1.45- 1.55 (2H, m),1.59-1.74 (4H, m), 2.40-2.49 (1H, m), 3.09 (2H, d, J = 7.3 Hz), 4.21(2H, d, J = 5.6 Hz), 6.88 (1H, s), 8.55 (1H, s), 9.85 (1H, t, J = 5.6Hz). 319 317 21 {[5-(3,5- difluorophenyl)-7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.8 Hz), 7.29 (s, 1H),7.56 (tt, 1H, J = 9.3, 2.3 Hz), 7.78-7.86 (m, 2H), 8.62 (s, 1H), 9.99(t, 1H, J = 5.8 Hz). 349 347 22 [(7-hydroxy-5- phenyl[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.12 (s, 1H),7.59-7.62 (m, 3H), 7.99-8.02 (m, 2H), 8.58 (s, 1H), 9.98 (t, 1H, J = 5.6Hz). 313 311 23 {[5-(3-chloro- 4- fluorophenyl)-7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.23 (s, 1H),7.67 (dd, 1H, J = 8.9, 8.9 Hz), 8.05 (ddd, 1H, J = 8.9, 2.4, 4.8 Hz),8.30 (dd, 1H, J = 7.3, 2.4 Hz), 8.60 (s, 1H), 9.98 (t, 1H, J = 5.4 Hz).365 363

TABLE 5 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 24 {[5-(3,3- dimethylbutyl)- 7-hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.98 (s, 9H), 1.59-1.70 (m, 2H), 3.01-3.13(m, 2H), 4.21 (d, 2H, J = 5.6 Hz), 6.89 (s, 1H), 8.57 (s, 1H), 9.84 (t,1H, J = 5.6 Hz). 321 319 25 {[5-(3,4- difluorophenyl)- 7-hydroxy[1,2,4]triazolo [1,5-a]pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.5 Hz), 7.22 (s, 1H),7.69 (dt, 1H, J = 15.0, 5.3 Hz), 7.92- 7.94 (m, 1H), 8.17 (ddd, 1H, J =11.9, 7.7, 2.2 Hz), 8.60 (s, 1H), 9.98 (t, 1H, J = 5.5 Hz). 349 347 26{[7-hydroxy-5- (p-tolyl) [1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.42 (s, 3H), 4.24 (d, 2H, J = 5.5 Hz),7.09 (s, 1H), 7.40 (d, 2H, J = 8.2 Hz), 7.93 (d, 2H, J = 8.2 Hz), 8.58(s, 1H), 9.97 (t, 1H, J = 5.5 Hz). 327 325 27 [(5- cyclohexyl-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.21- 1.62 (5H, m), 1.69-1.79 (1H, m),1.80- 1.88 (2H, m), 1.98-2.09 (2H, m), 3.31-3.43 (1H, m), 4.20 (2H, d, J= 5.8 Hz), 6.76 (1H, s), 8.56 (1H, s), 9.80- 9.87 (1H, m). 319 317 28[(5-cyclohexyl- methyl-7-hydroxy [1,2,4]triazolo [1,5-a]pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.98- 1.23 (5H, m), 1.56-1.70 (5H, m),1.90-1.99 (1H, m), 3.00 (2H, d, J = 7.2 Hz), 4.21 (2H, d, J = 5.6 Hz),6.84 (1H, s), 8.55 (1H, s), 9.85 (1H, t, J = 5.6 Hz). 333 331

TABLE 6 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 29 {[7-hydroxy-5- (3-phenylpropyl) [1,2,4]triazolo[1,5-a]pyridine- 8-carbonyl] amino}acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.07-2.15 (m, 2H), 2.71 (t, 2H, J = 7.7Hz), 3.12 (t, 2H, J = 7.6 Hz), 4.21 (d, 2H, J = 5.5 Hz), 6.85 (s, 1H),7.15-7.31 (m, 5H), 8.55 (s, 1H), 9.84 (t, 1H, J = 5.5 Hz). 355 353 30[(5- cyclopentyl-7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.68-1.84 (m, 6H), 2.14-2.21 (m, 2H),3.69-3.76 (m, 1H), 4.21 (d, 2H, J = 5.7 Hz), 6.83 (s, 1H), 8.56 (s, 1H),9.85 (t, 1H, J = 5.6 Hz). 305 303 31 {[5-(3-fluoro- 5- trifluoromethylphenyl)-7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino}acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.37 (s, 1H),7.99 (d, 1H, J = 9.3 Hz), 8.23 (d, 1H, J = 9.3 Hz), 8.30 (s, 1H), 8.63(s, 1H), 10.00 (t, 1H, J = 5.6 Hz). 399 397 32 {[5-(4- fluorophenyl)-7-hydroxy [1,2,4]triazolo [1,5-a]pyridine- 8-carbonyl] amino}acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (d, 2H, J = 5.7 Hz), 7.14 (s, 1H),7.41-7.48 (m, 2H), 8.07- 8.13 (m, 2H), 8.59 (s, 1H), 9.97 (t, 1H, J =5.7 Hz). 331 329 33 {[7-hydroxy-5- (3- trifluoromethyl phenyl) [1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.5 Hz), 7.28 (s, 1H),7.84 (t, 1H, J = 7.9 Hz), 7.98 (d, 1H, J = 7.9 Hz), 8.28 (d, 1H, J = 7.9Hz), 8.41 (s, 1H), 8.61 (s, 1H), 10.00 (t, 1H, J = 5.7 Hz). 381 379

TABLE 7 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 34 {[5-(2- fluoro-5- trifluoromethyl- phenyl)-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.28 (s, 1H),7.73 (dd, 1H, J = 9.1, 9.1 Hz), 8.10 (ddd, 1H, J = 9.1, 4.5, 2.0 Hz),8.24 (dd, 1H, J = 6.4, 2.0 Hz), 8.57 (s, 1H), 9.95 (t, 1H, J = 5.6 Hz).399 397 35 [(7-hydroxy- 5-isopropyl [1,2,4]triazolo [1,5-a]pyridine-8-carbonyl) amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.37 (d, 6H, J = 7.3 Hz), 3.67 (sept, 1H, J= 7.3 Hz), 4.21 (d, 2H, J = 5.6 Hz), 6.82 (s, 1H), 8.59 (s, 1H), 9.84(t, 1H, J = 5.6 Hz). 279 277 36 {[5-(3- chloro-5- trifluoromethyl-phenyl)-7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino}acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.37 (s, 1H),8.14 (s, 1H), 8.37 (s, 1H), 8.41 (s, 1H), 8.62 (s, 1H), 9.99 (t, 1H, J =5.6 Hz). 415 413 37 {[5-(3- cyanophenyl)- 7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.7 Hz), 7.28 (s, 1H),7.81 (t, 1H, J = 7.9 Hz), 8.08 (dt, 1H, J = 7.9, 1.0 Hz), 8.34 (d, 1H, J= 8.4 Hz), 8.48 (t, 1H, J = 1.3 Hz), 8.61 (s, 1H), 9.99 (t, 1H, J = 5.7Hz). 338 336 38 ({5-[2-(4- cyclopropyl- phenyl)ethyl]- 7-hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl}amino) acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.59-0.64 (m, 2H), 0.88-0.93 (m, 2H),1.83-1.90 (m, 1H), 3.06 (t, 2H, J = 7.9 Hz), 3.37 (t, 2H, J = 7.9 Hz),4.21 (d, 2H, J = 5.6 Hz), 6.81 (s, 1H), 6.99 (d, 2H, J = 8.1 Hz), 7.11(d, 2H, J = 8.1 Hz), 8.60 (s, 1H), 9.84 (t, 1H, J = 5.6 Hz). 381 379

TABLE 8 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 39 {[5-(2,2- dimethylpropyl)- 7-hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.97 (s, 9H), 3.12 (s, 2H), 4.21 (d, 2H, J= 5.6 Hz), 6.78 (s, 1H), 8.53 (s, 1H), 9.88 (t, 1H, J = 5.6 Hz). 307 30540 {[5-(1- ethylpropyl)- 7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.78 (t, 6H, J = 7.3 Hz), 1.72-1.94 (m,4H), 3.37-3.48 (m, 1H), 4.21 (d, 2H, J = 5.6 Hz), 6.85 (s, 1H), 8.55 (s,1H), 9.88 (t, 1H, J = 5.6 Hz). 307 305 41 {[5-(3-chloro-5-fluorophenyl)- 7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (d, 2H, J = 5.8 Hz), 7.28 (s, 1H),7.73 (dt, 1H, J = 8.7, 2.1 Hz), 7.88-7.91 (m, 1H), 7.98-8.00 (m, 1H),8.60 (s, 1H), 9.97 (t, 1H, J = 5.6 Hz). 365 363 42 {[5-(3-fluorophenyl)-7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.5 Hz), 7.21 (s, 1H),7.47 (tdd, 1H, J = 8.6, 2.6, 0.7 Hz), 7.64 (td, 1H, J = 8.1, 6.0 Hz),7.87 (dt, 1H, J = 7.8, 1.0 Hz), 7.90 (dt, 1H, J = 10.1, 2.1 Hz), 8.60(s, 1H), 9.99 (t, 1H, J = 5.4 Hz). 331 329 43 [(7-hydroxy-5-isobutyl[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.94 (d, 6H, J = 6.9 Hz), 2.28 (tsept, 1H,J = 6.9, 7.3 Hz), 2.98 (d, 2H, J = 7.3 Hz), 4.21 (d, 2H, J = 5.6 Hz),6.85 (s, 1H), 8.55 (s, 1H), 9.85 (t, 1H, J = 5.6 Hz). 293 291 44 {[5-(3-chlorophenyl)- 7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.22 (s, 1H),7.59-7.71 (m, 2H), 7.96 (d, 1H, J = 7.7 Hz), 8.11 (s, 1H), 8.59 (s, 1H),9.98 (br s, 1H), 12.99 (br s, 1H), 14.38 (br s, 1H). 347, 349 345, 347

TABLE 9 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 45 {[5-(2- ethylbutyl)-7- hydroxy[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.85 (t, 6H, J = 7.4 Hz), 1.25-1.39 (m,4H), 1.94-2.02 (m, 1H), 3.03 (d, 2H, J = 7.3 Hz), 4.21 (d, 2H, J = 5.5Hz), 6.87 (s, 1H), 8.56 (s, 1H), 9.85 (t, 1H, J = 5.5 Hz). 321 319 46{[5-(3,5- dichlorophenyl)- 7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 3H, J = 5.6 Hz), 7.30 (s, 1H),7.89 (t, 1H, J = 3.5 Hz), 8.08 (s, 1H), 8.09 (s, 1H), 8.61 (s, 1H), 9.99(t, 1H, J = 5.6 Hz). 381, 383 379, 381 47 {[5-(2- cyclopropyl- ethyl)-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.00-0.05 (2H, m), 0.35-0.42 (2H, m),0.72-0.81 (1H, m), 1.64-1.73 (2H, m), 4.20 (2H, d, J = 5.6 Hz), 6.86(1H, s), 8.55 (1H, s), 9.79-9.87 (1H, m). 305 303 48 {[5-(3,3-dimethylpentyl)- 7- hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (CD₃OD, 400 MHz) δ: 0.91 (t, 3H, J = 7.6 Hz), 0.98 (s, 6H), 1.39(q, 2H, J = 7.5 Hz), 1.70 (ddd, 2H, J = 8.7, 4.7, 3.8 Hz), 3.08-3.14 (m,2H), 4.24 (s, 2H), 6.82 (s, 1H), 8.54 (s, 1H). 335 333 49 {[7-hydroxy-5-(3,4,5- trifluorophenyl) [1,2,4]triazolo [1,5-a]pyridine- 8-carbonyl]amino}acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.5 Hz), 7.28 (s, 1H),8.09 (dd, 2H, J = 9.0, 6.8 Hz), 8.62 (s, 1H), 9.98 (t, 1H, J = 5.1 Hz).367 365 50 {[5-(4- chlorophenyl)- 7- hydroxy[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.17 (s, 1H),7.67 (d, 2H, J = 8.6 Hz), 8.05 (d, 2H, J = 8.6 Hz), 8.59 (s, 1H), 9.98(t, 1H, J = 5.6 Hz). 347 345

TABLE 10 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 51 [(7-hydroxy-5- (m-tolyl) [1,2,4]triazolo[1,5-a]pyridine- 8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.42 (3H, s), 4.24 (2H, d, J = 5.6 Hz),7.09 (1H, s), 7.41-7.51 (2H, m), 7.78-7.84 (2H, m), 8.58 (1H, s), 9.98(1H, t, J = 5.6 Hz). 327 325 52 {[5-(3- cyclopropyl-5- fluorophenyl)-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.82- 0.86 (m, 2H), 1.01-1.06 (m, 2H),2.03- 2.10 (m, 1H), 4.24 (d, 2H, J = 5.6 Hz), 7.15-7.18 (m, 1H), 7.20(s, 1H), 7.56 (dd, 1H, J = 1.4, 1.4 Hz), 7.62- 7.65 (m, 1H), 8.59 (s,1H), 9.98 (t, 1H, J = 5.6 Hz). 371 369 53 [(5-cyclobutyl- methyl-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.72- 1.90 (m, 4H), 1.98-2.10 (m, 2H),2.80- 2.92 (m, 1H), 3.20 (d, 2H, J = 7.4 Hz), 4.20 (d, 2H, J = 5.6 Hz),6.79 (s, 1H), 8.55 (s, 1H), 9.83 (t, 1H, J = 5.6 Hz). 305 303hydrochloride 54 {[5-(2- cyclobutylethyl)- 7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.54- 1.67 (m, 2H), 1.72-1.92 (m, 4H),1.95- 2.06 (m, 2H), 2.26-2.37 (m, 1H), 3.00 (t, 2H, J = 7.7 Hz), 4.21(d, 2H, J = 5.6 Hz), 6.85 (s, 1H), 8.56 (s, 1H), 9.85 (t, 1H, J = 5.6Hz). 319 317 55 {[5-(2-fluoro-3- trifluoromethyl phenyl)-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (2H, d, J = 5.6 Hz), 7.25 (1H, s),7.61- 7.68 (1H, m), 8.03-8.13 (2H, m), 8.57 (1H, s), 9.87-10.01 (1H, m).399 397

TABLE 11 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 56 {[5-(3-chloro- 2-fluorophenyl)- 7-hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (2H, d, J = 5.6 Hz), 7.21 (1H, s),7.47 (1H, dd, J = 7.9, 3.9 Hz), 7.73 (1H, dd, J = 7.1, 3.5 Hz), 7.88(1H, dd, J = 7.7, 3.8 Hz), 8.56 (1H, s), 9.95 (1H, t, J = 5.0 Hz). 365363 57 {[7-hydroxy-5- (4-trifluoromethyl phenyl) [1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (2H, d, J = 5.6 Hz), 7.23 (1H, s),7.96 (2H, d, J = 8.1 Hz), 8.21 (2H, d, J = 8.1 Hz), 8.59 (1H, s), 9.99(1H, t, J = 5.3 Hz). 381 379 58 [(5-cycloheptyl-7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.52- 1.86 (m, 10H), 1.96-2.04 (m, 2H),3.50-3.59 (m, 1H), 4.21 (d, 2H, J = 5.5 Hz), 6.78 (s, 1H), 8.56 (s, 1H),9.86 (t, 1H, J = 5.5 Hz). 333 331 59 {[5-(2,3- difluorophenyl)-7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.7 Hz), 7.20 (s, 1H),7.45 (tdd, 1H, J = 8.2, 4.9, 1.4 Hz), 7.59 (ddt, 1H, J = 8.3, 5.4, 1.2Hz), 7.70- 7.77 (m, 1H), 8.56 (s, 1H), 9.95 (t, 1H, J = 5.6 Hz). 349 34760 {[5-(2- cyclopentylethyl)- 7-hydroxy[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.11- 1.19 (m, 2H), 1.47-1.61 (m, 4H),1.74- 1.87 (m, 5H), 3.10 (t, 2H, J = 7.5 Hz), 4.21 (d, 2H, J = 5.6 Hz),6.87 (s, 1H), 8.56 (s, 1H), 9.84 (t, 1H, J = 5.6 Hz). 333 331

TABLE 12 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 61 {[5-(2- fluorophenyl)-7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.13 (s, 1H),7.41- 7.48 (m, 2H), 7.66-7.72 (m, 1H), 7.74-7.78 (m, 1H), 8.55 (s, 1H),9.95 (t, 1H, J = 5.6 Hz). 331 329 62 {[5-(4-chloro- 2-fluorophenyl)- 7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.2 Hz), 7.16 (s, 1H),7.55 (dd, 1H, J = 8.1, 1.4 Hz), 7.74 (dd, 1H, J = 10.0, 1.4 Hz), 7.81(dd, 1H, J = 8.1, 8.1 Hz), 8.56 (s, 1H), 9.94 (t, 1H, J = 5.2 Hz). 365363 63 {[5-(4- fluorobenzyl)-7- hydroxy[1,5-a] pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.20 (2H, d, J = 5.5 Hz), 4.46 (2H, s),6.74 (1H, s), 7.16 (2H, dd, J = 8.9, 4.5 Hz), 7.45 (2H, dd, J = 8.6, 5.5Hz), 8.57 (1H, s), 9.83 (1H, t, J = 5.4 Hz). 345 343 64 (R)-2-{[5-(3,5-difluorophenyl)- 7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} propionic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.52 (d, 3H, J = 7.1 Hz), 4.58-4.67 (m,1H), 7.28 (br s, 1H), 7.51-7.59 (m, 1H), 7.81 (d, 2H, J = 6.4 Hz), 8.62(s, 1H), 10.08-10.15 (br m, 1H). 363 361 65 [(7-hydroxy-5- propyl[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.97 (t, 3H, J = 7.4 Hz), 1.80 (tq, 2H, J =7.4, 7.4 Hz), 3.07 (t, 2H, J = 7.4 Hz), 4.21 (d, 1H, J = 5.7 Hz), 6.85(s, 1H), 8.56 (s, 1H), 9.84 (t, 1H, J = 5.7 Hz). 279 277

TABLE 13 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 66 2-{[5-(3,5- difluorophenyl)- 7-hydroxy-[1,2,4]triazolo [1,5-a]pyridine- 8-carbonyl] amino}propionic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.52 (d, 3H, J = 7.1 Hz), 4.58-4.67 (m,1H), 7.28 (br s, 1H), 7.51-7.59 (m, 1H), 7.81 (d, 2H, J = 6.4 Hz), 8.62(s, 1H), 10.08- 10.15 (br m, 1H). 363 361 67 (S)-2-{[5-(3,5-difluorophenyl)- 7-hydroxy[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl]amino} propionic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.52 (d, 3H, J = 7.1 Hz), 4.60-4.67 (m,1H), 7.31 (s, 1H), 7.56 (t, 1H, J = 9.3 Hz), 7.82 (d, 2H, J = 6.6 Hz),8.61 (s, 1H), 10.10 (d, 1H, J = 6.6 Hz), 13.16 (br s, 1H), 14.32 (s,1H). 363 361 68 2-{[5-(3,5- difluorophenyl)-7- hydroxy[1,2,4]triazolo[1,5-a] pyridine-8- carbonyl]amino}- 2- methylpropanoic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.63 (s, 6H), 7.27 (s, 1H), 7.51-7.60 (m,1H), 7.76-7.83 (m, 2H), 8.61 (s, 1H), 10.15 (s, 1H). 377 375 69(S)-2-[(7- hydroxy-5- phenethyl[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl)amino] propionic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.49 (d, 3H, J = 7.3 Hz), 3.12 (t, 2H, J =7.8 Hz), 3.41 (t, 2H, J = 7.8 Hz), 4.56-4.63 (m, 1H), 6.81 (s, 1H),7.18-7.33 (m, 5H), 8.61 (s, 1H), 9.97 (d, 1H, J = 7.1 Hz). 355 353 70(R)-2-[(7- hydroxy-5- phenethyl[1,2,4] triazolo[1,5-a] pyridine-8-carbonyl)amino] propionic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.49 (d, 3H, J = 7.3 Hz), 3.12 (t, 2H, J =7.8 Hz), 3.41 (t, 2H, J = 7.8 Hz), 4.56- 4.63 (m, 1H), 6.80 (s, 1H),7.18-7.33 (m, 5H), 8.61 (s, 1H), 9.97 (d, 1H, J = 7.1 Hz). 355 353

TABLE 14 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 71 [(7-hydroxy-6- pentyl[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.87 (t, 3H, J = 6.9 Hz), 1.28-1.36 (m,4H), 1.61 (t, 2H, J = 7.6 Hz), 2.62 (t, 2H, J = 7.6 Hz), 4.21 (d, 2H, J= 5.3 Hz), 8.50 (s, 1H), 8.88 (s, 1H), 9.93 (s, 1H), 14.81 (s, 1H). 307305 72 {[7-hydroxy-5- (5-methyl- thiophen-2- yl)[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.58 (s, 3H), 4.23 (d, 2H, J = 5.5 Hz),7.07 (d, 1H, J = 3.7 Hz), 7.50 (s, 1H), 8.27 (d, 1H, J = 4.0 Hz), 8.67(s, 333 331 1H), 9.85-9.90 (br m, 1H). 73 [(5-hexyl-7- hydroxy[1,2,4]triazolo[1,5- a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.85 (3H, t, J = 7.0 Hz), 1.23-1.41 (6H,m), 1.71- 1.81 (2H, m), 3.08 (2H, t, J = 321 319 7.7 Hz), 4.20 (2H, d, J= 5.6 Hz), 6.85 (1H, s), 8.56 (1H, s), 9.79-9.86 (1H, m). 74[(7-hydroxy-5- pentyl[1,2,4] triazolo[1,5- a]pyridine-8- carbonyl)amino]acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.84- 0.91 (m, 3H), 1.29-1.40 (m, 4H),1.72-1.83 (m, 2H), 3.09 (t, 2H, J = 7.5 Hz), 4.21 (d, 307 305 2H, J =5.4 Hz), 6.86 (s, 1H), 8.56 (s, 1H), 9.83 (t, 1H, J = 5.4 Hz). 75{[5-(2,5- difluorophenyl)- 7-hydroxy[1,2,4] triazolo[1,5- a]pyridine-8-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.6 Hz), 7.19 (s, 1H),7.49-7.60 (m, 2H), 7.67- 7.73 (m, 1H), 8.56 (s, 1H), 9.95 (t, 1H, J =5.6 Hz). 349 347

TABLE 15 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 76 {[7-hydroxy-5- (2,3,5- trifluorophenyl)[1,2,4]triazolo [1,5-a]pyridine- 8-carbonyl] amino) acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.5 Hz), 7.25 (s, 1H),7.58-7.64 (m, 1H), 7.86- 7.93 (m, 1H), 8.59 (s, 1H), 9.95 (t, 1H, J =5.5 Hz). 367 365 77 {[5-(2,4- difluorophenyl)- 7-hydroxy [1,2,4]triazolo[1,5- a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.2 Hz), 7.14 (s, 1H),7.30-7.39 (m, 1H), 7.50- 7.60 (m, 1H), 7.81-7.89 (m, 1H), 8.55 (s, 1H),9.94 (t, 1H, J = 5.4 Hz). 349 347 78 {[5-(4-chloro-3- fluorophenyl)-7-hydroxy[1,2,4] triazolo[1,5- a]pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (d, 2H, J = 5.6 Hz), 7.26 (s, 1H),7.82-7.86 (m, 1H), 7.93 (dd, 1H, J = 8.5, 1.6 Hz), 8.13 (dd, 1H, J =10.5, 2.0 Hz), 8.61 (s, 1H), 9.98 (t, 1H, J = 5.4 Hz). 365 363 79{[5-(3-fluoro-5- methylphenyl)-7- hydroxy[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.43 (s, 3H), 4.25 (d, 2H, J = 5.3 Hz),7.18 (s, 1H), 7.32 (d, 1H, J = 9.3 Hz), 7.70 (d, 2H, J = 10.4 Hz), 8.60(d, 1H, J = 0.7 Hz), 9.99 (t, 345 343 1H, J = 5.3 Hz). 80 [(6-chloro-7-hydroxy-5- phenethyl[1,2,4] triazolo[1,5- a]pyridine-8- carbonyl)amino]acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.05 (t, 2H, J = 7.8 Hz), 3.56 (t, 2H, J =7.8 Hz), 4.17 (d, 2H, J = 5.1 Hz), 7.16-7.22 (m, 3H), 7.23- 7.29 (m,2H), 375 373 8.60 (s, 1H). 81 [(6-chloro-7- hydroxy-5- propyl[1,2,4]triazolo[1,5- a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.09 (t, 2H, J = 7.8 Hz), 3.28 (t, 2H, J =7.8 Hz), 4.25 (d, 2H, J = 5.6 Hz), 7.16-7.32 (m, 5H), 7.36 313 311 (s,1H), 8.68 (s, 1H), 10.42 (t, 1H, J = 5.6 Hz), 13.26 (s, 1H).

TABLE 16 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 82 {[5-(4- cyclcpropyl-2- fluorophenyl)-7-hydroxy[1,2,4] triazolo[1,5- a]pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.82- 0.86 (m, 2H), 1.05-1.10 (m, 2H),2.04-2.11 (m, 1H), 4.24 (d, 2H, J = 5.6 Hz), 7.06 (s, 1H), 7.14 (d, 1H,J = 8.1 Hz), 7.15 (d, 1H, J = 7.7 371 369 Hz), 7.62 (dd, 1H, J = 7.7,7.7 Hz), 8.53 (s, 1H), 9.94 (t, 1H, J = 5.6 Hz). 83 [(6-hydroxy-8-phenyl[1,2,4] triazolo[1,5- a]pyridine-5- carbbonyl)amino] acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.5 Hz), 7.50-7.63 (m,3H), 7.80 (s, 1H), 8.21 (d, 2H, J = 7.3 Hz), 8.74 (s, 1H), 10.53 (t, 1H,J = 5.5 313 311 Hz), 13.36 (s, 1H). 84 {[8-(3-chloro- phenyl)-6-hydroxy[1,2,4] triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.6 Hz), 7.58-7.64 (m,2H), 7.92 (s, 1H), 6.15- 8.21 (m, 1H), 8.37-8.39 (m, 1H), 8.76 (s, 1H),10.54 (t, 347 345 1H, J = 5.4 Hz), 13.06 (s, 1H), 13.36 (s, 1H). 85{[8-(3,5- difluorophenyl)- 6-hydroxy[1,2,4] triazolo[1,5- a]pyridine-5-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.6 Hz), 7.47 (tt, 1H, J =9.3, 2.3 Hz), 8.03 (s, 1H), 8.06- 8.14 (m, 2H), 8.78 (s, 1H), 10.54 (t,1H, J = 5.4 Hz), 13.35 (s, 1H). 349 347 86 [(8-benzyl-6- hydroxy[1,2,4]triazolo[1,5- a]pyridine-5- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (d, 2H, J = 5.6 Hz), 4.33 (s, 2H),7.20-7.25 (m, 1H), 7.28- 7.33 (m, 2H), 327 325 7.35 (s, 1H), 7.38-7.41(m, 2H), 8.66 (s, 1H), 10.40 (t, 1H, J = 5.6 Hz), 13.27 (s, 1H).

TABLE 17 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 87 [(6-hydroxy-8- phenethyl[1,2,4] triazolo[1,5-a]pyridine-5- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.09 (t, 2H, J = 7.8 Hz), 3.28 (t, 2H, J =7.8 Hz), 4.25 (d, 2H, J = 5.6 Hz), 7.16-7.32 (m, 5H), 7.36 (s, 1H), 8.68341 339 (s, 1H), 10.42 (t, 1H, J = 5.6 Hz), 13.26 (s, 1H). 88{[8-(2-chloro- phenyl)-6- hydroxy[1,2,4] triazolo[1,5- a]pyridine-5-carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.6 Hz), 7.49-7.59 (m,2H), 7.60- 7.63 (m, 2H), 7.67 (dd, 1H, J = 7.9, 1.4 Hz), 8.66 (s, 1H),10.50 (t, 1H, J = 347 345 5.6 Hz), 13.06 (s, 1H), 13.37 (s, 1H). 89{[8-(3,5- dichloro- phenyl)-6- hydroxy[1,2,4] triazolo[1,5-a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.3 Hz), 7.80 (t, 1H, J =1.9 Hz), 8.03 (s, 1H), 8.36 (d, 2H, J = 1.8 Hz), 8.77 (s, 1H), 10.53 (t,1H, J = 5.3 Hz), 13.34 (s, 381 379 1H). 90 ({8-[2-{4- fluorophenyl)ethyl]-6- hydroxy[1,2,4] triazolo[1,5- a]pyridine-5- carbonyl}amino)acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.09 (t, 2H, J = 7.9 Hz), 3.27 (t, 2H, J =7.7 Hz), 4.25 (d, 2H, J = 5.5 Hz), 7.10 (t, 2H, J = 8.9 Hz), 7.26 (dd,359 357 2H, J = 8.7, 5.8 Hz), 7.35 (s, 1H), 8.66 (s, 1H), 10.42 (t, 1H,J = 5.3 Hz), 13.26 (s, 1H). 91 [(8-cyclo- hexylmethyl-6- hydroxy[1,2,4]triazolo[1,5- a]pyridine-5- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.94- 1.23 (m, 5H), 1.53-1.70 (m, 5H),1.80-1.94 (m, 1H), 2.86 (d, 2H, J = 7.2 Hz), 4.25 (d, 333 331 2H, J =5.6 Hz), 7.36 (s, 1H), 8.62 (s, 1H), 10.42 (t, 1H, J = 5.6 Hz), 13.28(s, 1H).

TABLE 18 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 92 [(8-cyclahexyl- 6-hydroxy [1,2,4] triazolo[1,5-a]pyridine-5- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.23- 1.34 (m, 1H), 1.38-1.49 (m, 2H),1.57-1.67 (m, 2H), 1.73- 1.77 (m, 1H), 1.82-1.86 (m, 2H), 1.91-1.96 (m,2H), 3.15- 319 317 3.22 (m, 1H), 4.25 (d, 2H, J = 5.6 Hz), 7.33 (s, 1H),8.63 (s, 1H), 10.42 (t, 1H, J = 5.6 Hz), 13.29 (s, 1H). 93[(8-cyclohex-1- enyl-6- hydroxy[1,2,4] triazolo[1,5- a]pyridine-5-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.62- 1.68 (m, 2H), 1.74-1.80 (m, 2H),2.31-2.35 (m, 2H), 2.49- 2.54 (m, 2H), 4.25 (d, 2H, J = 5.6 Hz), 7.33(s, 1H), 7.58- 317 315 7.61 (m, 1H), 8.66 (s, 1H), 10.48 (t, 1H, J = 5.6Hz), 13.28 (s, 1H). 94 {[8-(3-chloro- 4-fluoro- phenyl)-6-hydroxy[1,2,4] triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.5 Hz), 7.64 (t, 1H, J =8.9 Hz), 7.94 (s, 1H), 8.29 (dq, 1H, J = 8.7, 2.3 Hz), 8.57 (dd, 1H, J =365 363 7.2, 2.3 Hz), 8.77 (s, 1H), 10.52 (t, 1H, J = 5.5 Hz), 13.36 (s,1H). 95 {[8-(3,4- dichlorophenyl)- 6-hydroxy[1,2,4] triazolo[1,5-a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.5 Hz), 7.84 (d, 1H, J =8.4 Hz), 7.97 (s, 1H), 8.25 (dd, 1H, J = 8.4, 2.2 Hz), 8.60 (d, 1H, J =2.2 381 379 Hz), 8.77 (s, 1H), 10.52 (t, 1H, J = 5.5 Hz), 13.35 (s, 1H).

TABLE 19 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 96 {[8-(5- chlorothiophen- 2-yl)-6- hydroxy[1,2,4]triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.26 (d, 2H, J = 5.5 Hz), 7.35 (d, 1H, J =4.2 Hz), 8.06 (s, 1H), 8.22 (d, 1H, J = 4.2 Hz), 8.78 (s, 1H), 10.41 (t,1H, J = 5.5 Hz), 13.35 353 351 (s, 1H). 97 {[8-(3,5-bis- trifluoromethylphenyl)-6- hydroxy[1,2,4] triazolo[1,5- a]pyridine-5- carbonyl]amino}acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4-29 (d, 2H, J = 5.5 Hz), 8.24 (s, 1H),8.29 (s, 1H), 8.82 (s, 1H), 8.98 (s, 2H), 10.55 (t, 1H, J = 5.5 Hz),13.36 (s, 1H). 449 447 98 {[8-(2-cyclo- hexylethyl)-6- hydroxy[1,2,4]triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.85- 1.34 (m, 6H), 1.53-1.82 (m, 7H),2.94-3.02 (m, 2H), 4.25 (d, 2H, J = 5.6 Hz), 7.40 (s, 1H), 8.63 (s, 1H),10.41 (t, 1H, J = 5.6 Hz), 13.28 347 345 (s, 1H). 99 {[8-(2-cyclo-pentylethyl)-6- hydroxy[1,2,4] triazolo[1,5- a]pyridine-5-carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 1.07- 1.22 (m, 2H), 1.41-1.65 (m, 4H),1.70-1.86 (m, 5H), 2.93- 3.02 (m, 2H), 4.25 (d, 2H, J = 5.6 Hz), 7.40(s, 1H), 8.64 (s, 333 331 1H), 10.41 (t, 1H, J = 5.6 Hz), 13.28 (s, 1H).100  ({6-hydroxy-8- [2-(2- trifluoromethyl phenyl)ethyl] [1,2,4]triazolo[1,5-a]pyridine-5- carbonyl}amino) acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.21- 3.35 (m, 4H), 4.25 (d, 2H, J = 5.6Hz), 7.38 (s, 1H), 7.44 (t, 1H,) J = 7.5 Hz), 7.56 (d, 1H, J = 7.7 Hz),7.63 (t, 1H, J = 7.7 Hz), 7.70 (d, 1H, J = 7.5 Hz), 8.68 (s, 409 4071H), 10.43 (t, 1H, J = 5.6 Hz), 13.28 (s, 1H).

TABLE 20 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 101 ({6-hydroxy-8- [2-(3- trifluoromethyl phenyl)ethyl][1,2,4]triazolo [1,5-a]pyridine- 5-carbonyl} amino) acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.20 (dd, 2H, J = 9.4, 6.5 Hz), 3.32 (dd,2H, J = 9.4, 6.5 Hz), 4.25 (d, 2H, J = 5.6 Hz), 7.40 (s, 1H), 7.49- 7.59(m, 3H), 7.63 (s, 1H), 8.68 (s, 1H), 10.42 (t, 1H, J = 409 407 5.6 Hz),13.27 (s, 1H). 102 ({6-hydroxy-8- [2-(4- trifluoromethyl phenyl)ethyl][1,2,4]triazolo [1,5-a]pyridine- 5-carbonyl} amino) acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.17- 3.24 (m, 2H), 3.28-3.36 (m, 2H), 4.25(d, 2H, J = 5.6 Hz), 7.40 (s, 1H), 7.48 (d, 2H, J = 7.9 Hz), 7.65 (d,2H, J = 7.9 409 407 Hz), 8.68 (s, 1H), 10.42 (t, 1H, J = 5.6 Hz), 13.27(s, 1H). 103 {[8-(3-chloro-5- cyclopropyl- phenyl)-yl)-6- hydroxy[1,2,4]triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.84- 0.90 (m, 2H), 1.01-1.06 (m, 2H),2.03-2.10 (m, 1H), 4.28 (d, 2H, J = 5.4 Hz), 7.31 (dd, 1H, J = 1.8, 1.8Hz), 7.83 (dd, 1H, J = 1.8, 1.8 Hz), 7.93 (s, 1H), 387 385 8.13 (dd, 1H,J = 1.8, 1.8 Hz), 8.75 (s, 1H), 10.53 (t, 1H, J = 5.4 Hz), 13.35 (s,1H). 104 {[8-(3-fluoro-5- trifluoromethyl phenyl)-6- hydroxy[1,2,4]triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.29 (d, 2H, J = 5.5 Hz), 7.89 (d, 1H, J =8.6 Hz), 8.12 (s, 1H), 8.46 (d, 1H, J = 8.6 Hz), 8.63 (s, 1H), 8.80 (s,1H), 10.54 (t, 399 397 1H, J = 5.5 Hz), 13.36 (s, 1H). 105{[8-(3-chloro-5- fluorophenyl)-6- hydroxy[1,2,4] triazolo[1,5-a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.28 (d, 2H, J = 5.3 Hz), 7.62-7.67 (m,1H), 8.03 (s, 1H), 8.13- 8.19 (m, 1H), 8.31 (s, 1H), 8.78 (s, 1H), 10.54(t, 1H, J = 5.3 Hz), 365 363 13.35 (s, 1H).

TABLE 21 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) M − H) 106 {[8-(4-fluoro-3- trifluoromethyl phenyl)-6-hydroxy[1,2,4] triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.29 (d, 2H, J = 5.6 Hz), 7.71-7.80 (m,1H), 8.03 (s, 1H), 8.56- 8.63 (m, 1H), 8.73-8.82 (m, 2H), 10.53 (t, 1H,J = 5.6 Hz), 13.37 (s, 399 397 1H). 107 [(6-hydroxy [1,2,4]triazolo[1,5- a]pyridine-5- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.27 (d, 2H, J = 5.3 Hz), 7.56 (d, 1H, J =9.7 Hz), 8.09 (d, 1H, J = 9.7 Hz), 8.68 (s, 1H), 10.49 (t, 1H, J = 5.3237 235 Hz), 13.29 (br, s, 1H). 108 {[8-(4-chloro- phenyl)-6-hydroxy[1,2,4] triazolo[1,5- a]pyridine-5- carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (d, 2H, J = 5.2 Hz), 7.62-7.67 (m,2H), 7.86 (s, 1H), 8.26- 8.31 (m, 2H), 8.74 (s, 1H), 10.53 (t, 1H, J =5.2 Hz), 13.31 347 345 (br s, 1H). 109 ({8-[2-(3,5- difluoro-phenyl)ethyl]- 6-hydroxy [1,2,4]triazolo [1,5-a]pyridine- 5-caxbonyl}amino) acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.13 (t, 2H, J = 7.9 Hz), 3.30 (t, 2H, J =7.9 Hz), 4.25 (d, 2H, J = 5.2 Hz), 6.98-7.08 (m, 3H), 7.40 (s, 1H), 8.67(s, 1H), 10.42 (t, 1H, J = 5.2 377 375 Hz), 13.27 (br s, 1H). 110{[6-hydroxy-8- (3-trifluoromethyl phenyl)[1,2,4] triazolo[1,5-a]pyridine-5- carbonyl]amino} acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.29 (d, 2H, J = 5.5 Hz), 7.82 (t, 1H, J =7.9 Hz), 7.91 (d, 1H, J = 7.9 Hz), 8.00 (s, 1H), 8.48 (d, 1H, J = 7.9381 379 Hz), 8.70 (s, 1H), 8.78 (s, 1H), 10.54 (t, 1H, J = 5.5 Hz),13.36 (br s, 1H).

TABLE 22 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 111 [(7-hydroxy- 3,6- diphenyl[1,2,4] triazolo[4,3-a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.09 (d, 2H, J = 5.5 Hz), 7.36-7.44 (m,3H), 7.57- 7.66 (m, 5H), 7.90 (d, 2H, J = 7.3 Hz), 8.00 (s, 1H), 10.56(t, 1H, J = 5.3 Hz), 12.61 (s, 1H), 13.95 (s, 1H). 389 387 112[(7-hydroxy-3- methyl-6- phenyl[1,2,4] triazolo[4,3- a]pyridine-8-carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 2.62 (s, 3H), 4.05 (d, 2H, J = 5.5 Hz),7.39-7.46 (m, 3H), 7.63 (d, 2H, J = 6.8 Hz), 8.21 (s, 1H), 10.54 (t, 1H,J = 5.3 Hz), 12.58 (s, 1H), 13.44 (s, 1H). 327 325 113 [(7-hydroxy-3-phenyl[1,2,4] triazolo[4,3- a]pyridine-8- carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.06- 4.24 (m, 2H), 6.47-6.74 (m, 1H),7.58-7.71 (m, 3H), 7.78- 7.89 (m, 2H), 313 311 7.99-8.42 (m, 1H),9.99-10.43 (m, 1H). 114 [(7-hydroxy-3- phenethyl[1,2,4] triazolo[4,3-a]pyridine-8- carbonyl)amino] acetic acid hydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.08 (t, 2H, J = 7.7 Hz), 3.28 (t, 2H, J =7.7 Hz), 4.05 (d, 2H, J = 5.2 Hz), 6.46 (d, 1H, J= 7.3 341 339 Hz),7.16-7.25 (m, 1H), 7.26- 7.32 (m, 4H), 8.19 (d, 1H, J = 7.3 Hz), 10.33(br s, 1H), 13.52 (br s, 1H). 115 {[3-(2-cyclo- hexylethyl)-7-hydroxy[1,2,4] triazolo[4,3- a]pyridine-8- carbonyl]amino} acetic acidhydrochloride

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.90- 0.98 (m, 2H), 1.17-1.22 (m, 3H),1.28-1.40 (m, 1H), 1.62- 1.67 (m, 5H), 1.75-1.78 (m, 2H), 2.96 (t, 2H, J= 7.9 347 345 Hz), 4.04 (d, 2H, J = 5.2 Hz), 6.52 (d, 1H, J = 7.7 Hz),8.21 (d, 1H, J = 7.7 Hz), 10.28 (br s, 1H).

TABLE 23 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 116 [(7-hydroxy-5- phenethyl[1,2,4] triazolo[1,5-a]pyridine-8- carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 3.12 (t, 2H, J = 7.9 Hz), 3.40 (t, 3H, J =7.9 Hz), 4.22 (d, 2H, J = 5.2 Hz), 6.79 (s, 1H), 7.21- 7.29 (m, 5H),8.58 (s, 1H), 9.84 (t, 1H, J = 5.2 Hz), 341 339 12.97 (s, 1H), 14.22 (s,1H). 117 [(5-butyl-7- hydroxy[1,2,4] triazolo[1,5- a]pyridine-8-carbonyl)amino] acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.93 (t, 3H, J = 7.5 Hz), 1.33-1.44 (m,2H), 1.71-1.80 (m, 2H), 3.10 (t, 2H, J = 7.5 Hz), 4.20 (d, 293 291 2H, J= 5.2 Hz), 6.85 (s, 1H), 8.55 (s, 1H), 9.84 (br s, 1H), 14.26 (br s,1H). 118 {[5-(3-fluoro-5- trifluoromethyl phenyl)-7- hydroxy[1,2,4]triazolo[1,5- a]pyridine-8- carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.25 (d, 2H, J = 5.1 Hz), 7.39 (s, 1H),7.99 (d, 1H, J = 8.6 Hz), 8.23 (d, 1H, J = 9.5 Hz), 8.31 (s, 1H), 8.62(s, 1H), 9.98 (s, 1H), 13.01 (s, 1H), 14.41 (s, 1H). 399 397 119[(7-hydroxy-5- pentyl[1,2,4] triazolo[1,5- a]pyridine-8- carbonyl)amino]acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.88 (t, 3H, J = 7.6 Hz), 1.28-1.40 (m,4H), 1.73-1.83 (m, 2H), 3.09 (t, 2H, J = 7.6 Hz), 4.21 (d, 307 305 2H, J= 5.5 Hz), 6.85 (s, 1H), 8.54 (s, 1H), 9.84 (t, 1H, J = 5.5 Hz), 12.94(s, 1H), 14.25 (s, 1H).

TABLE 24 Ex. MS MS No. compound name structural formula ¹H-NMR, δ ppm(M + H) (M − H) 120 {[5-(3-chloro- phenyl)-7- hydroxy[1,2,4]triazolo[1,5- a]pyridine-8- carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (d, 2H, J = 5.3 Hz), 7.22 (s, 1H),7.58- 7.70 (m, 2H), 7.96 (d, 1H, J = 7.7 Hz), 8.11 (s, 1H), 8.59 (s,1H), 9.97 (s, 1H), 14.38 (s, 1H). 347 345 121 {[5-(4-fluoro-3-trifluoromethyl phenyl)-7- hydroxy[1,2,4] triazolo[1,5- a]pyridine-8-carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 4.24 (2H, d, J = 5.6 Hz), 7.30 (1H, s),7.77 (1H, dd, J = 10.5, 9.3 Hz), 8.36-8.40 (1H, m), 8.47 (1H, d, J = 6.9Hz), 8.60 (1H, s), 9.97 (1H, br s), 14.38 399 397 (1H, br s). 122{[5-(3- cyclopropyl-5- fluorophenyl)- 7-hydroxy [1,2,4] triazolo[1,5-a]pyridine-8- carbonyl]amino} acetic acid

¹H-NMR (DMSO-D₆, 400 MHz) δ: 0.81-0.87 (m, 2H), 1.00-1.07 (m, 2H),2.03-2.10 (m, 1H), 4.22 (d, 2H, J = 5.6 Hz), 7.13-7.23 (m, 2H), 7.56 (s,1H), 7.63 (d, 1H, J = 9.3 Hz), 8.58 (s, 1H), 9.99 (s, 1H), 14.36 (s,1H). 371 369

Examples of the Formulation Example of the present invention include thefollowing formulations. However, the present invention is not limited bysuch Formulation Examples.

Formulation Example 1 Production of Capsule

1) compound of Example 1 30 mg 2) microcrystalline cellulose 10 mg 3)lactose 19 mg 4) magnesium stearate  1 mg

1), 2), 3) and 4) are mixed and filled in a gelatin capsule

Formulation Example 2 Production of Tablet

1) compound of Example 1 10 g 2) lactose 50 g 3) cornstarch 15 g 4)carmellose calcium 44 g 5) magnesium stearate  1 g

The total amount of 1), 2), 3) and 30 g of 4) are kneaded with water,vacuum dried and sieved. The sieved powder is mixed with 14 g of 4) and1 g of 5), and the mixture is tableted by a tableting machine. In thisway, 1000 tablets containing 10 mg of the compound of Example 1 pertablet are obtained.

Next, the evaluation methods of the human PHD inhibitory activity andhuman EPO production-inducing activity of the compound of the presentinvention or a pharmaceutically acceptable salt thereof, or a solvatethereof are explained.

Experimental Example 1 Measurement of Human PHD Inhibitory Activity i)Expression and Purification of Human PHD2

Human PHD2 was expressed in insect cell (Sf9 cell). FLAG-tag wasinserted into the N-terminal in the translational region of humanPHD2-registered sequence (NM_022051), and the sequence was introducedinto a pVL1393 vector, and the sequence was confirmed. The vector andbaculovirus were cotransfected into Sf9, and human PHD2 expressionbaculovirus was isolated in Sf9. By using the virus, humanPHD2-expressed cell was prepared. After the cell was cultured at 27° C.for 72 hr, cell lysing solution containing various protease inhibitorswas added, and the cell was disrupted by sonication. The cell lysate wasflowed into a column filled with ANTI-FLAG M2 Affinity Gel Freezer Safe(SIGMA), washed, and the N-terminal FLAG-tag-added human PHD2 was elutedand collected. The purification product was confirmed to be human PHD2enzyme by Western-Blotting using an anti-FLAG antibody and an anti-PHD2antibody.

ii) Expression and Purification of VBC Complex

VBC complex (VHL/Elongin B/Elongin C) was expressed in Escherichia coli(BL21(DE3)). GST-fusion was inserted into the N-terminal in thetranslational region of human VHL-registered sequence (NM_000551).FLAG-tag was inserted into the N-terminal in the translational region ofhuman Elongin B-registered sequence (NM_207013), and the sequences wereintroduced into a pETDuet-1 vector, and the sequences were confirmed.His-tag was inserted into the N-terminal in the translational region ofhuman Elongin C-registered sequence (NM_005648), and the sequence wasintroduced into a pRSFDuet-1 vector, and the sequence was confirmed.After these expression vectors were transfected into Escherichia coli(BL21(DE3)), Escherichia coli was cultured at 37° C. in the mediumcontaining IPTG. The collected Escherichia coli was disrupted bysonication and flowed into a column filled with Ni-NTA superflow(QIAGEN), washed, and the product was eluted and collected. The eluatewas flowed into a column filled with Glutathione Sepharose 4B, washed,and the product was eluted and collected. The purification product wasconfirmed to be human VHL•human Elongin B and human Elongin C byWestern-Blotting using an anti-GST antibody•an anti-FLAG antibody and ananti-His antibody.

iii) Binding Activity of VBC Complex

The binding activity of the VBC complex obtained in the aforementionedii) to 19 residues of Biotin-labeled partial peptide (HIF-1α-C19) basedon the sequence of HIF-1α or Biotin-labeled partial peptide (HIF-1α-C19(Hyp)) wherein proline residue in said sequence is hydroxylated wasmeasured on streptavidin Coated Plate. For detection, ELISA using ananti-GST antibody was performed, and binding of VBC complex only tohydroxylated HIF-1α partial peptide was confirmed.

iv) Measurement of Human PHD Inhibitory Activity

As for human PHD2 enzyme activity, hydroxylation of proline residuecontained in the 19 residues of the partial peptide based on thesequence of HIF-1α as a substrate was measured by TR-FRET (Time-ResolvedFluorescence Resonance Energy Transfer) method.

The enzyme and substrate were each diluted with 50 mM tris-hydrochloridebuffer (pH 7.5) containing 50 μM iron sulfate, 120 mM NaCl, 0.1% BSA,0.1 mM ascorbic acid, 10 μM 2-oxoglutaric acid, 0.2 mM CHAPS, and thetest compound was diluted with dimethyl sulfoxide (DMSO).

A test compound and a substrate solution were added to a 96-well plate.The reaction was started by addition of a human PHD2 enzyme solution(final concentration 1 nM) to the reaction system. After incubation at25° C. for 30 min, a stop solution containing EDTA was added, and a VBCcomplex solution containing europium (Eu) and Xlent was added, and theamount of hydroxylated proline residue was quantified by time-resolvedfluorescence spectroscopy. The time-resolved fluorescence in each wellwas measured, and the human PHD inhibitory activity (%) of the testcompound was calculated based on the values of enzyme non-addition welland test compound non-addition well. The human PHD inhibitory activityof each compound is shown by IC₅₀ (μM) or as human PHD inhibitoryactivity (%) at 30 μM in the following Tables 25 to 29. In these Tables,the values consisting solely of numbers show IC₅₀ (μM) and thosecontaining % show human PHD inhibitory activity (%) at 30 μm.

TABLE 25 Ex. IC₅₀ (μM) or inhibitory activity No. (%) at 30 μM in vitro1 0.42 2 0.22 3 0.45 4 7.15 5 1.17 6 0.87 7 1.59 8 0.49 9 1.57 10 1.3311 0.29 12 0.82 13 1.31 14 0.23 15 1.80 16 0.32 17 0.29 18 0.48 19 0.2620 0.59 21 0.25 22 0.21 23 0.19 24 0.57 25 0.25 26 0.33 27 0.74 28 1.3829 0.92

TABLE 26 Ex. IC₅₀ (μM) or inhibitory activity No. (%) at 30 μM in vitro30 0.98 31 0.80 32 0.38 33 0.46 34 0.43 35 0.88 36 0.72 37 0.20 38 0.5939 1.25 40 0.87 41 0.26 42 0.24 43 0.93 44 0.20 45 0.92 46 0.29 47 0.5648 0.59 49 0.24 50 0.18 51 0.26 52 0.89 53 0.50 54 0.44 55 0.23 56 0.1957 0.20 58 0.55

TABLE 27 Ex. IC₅₀ (μM) or inhibitory activity No. (%) at 30 μM in vitro59 0.26 60 0.74 61 0.22 62 0.28 63 0.36 64 6.88 65 0.72 66 1.50 67 0.9068 5.94 69 1.62 70 38% 71 2.47 72 0.40 73 7.09 74 0.85 75 0.21 76 0.2277 0.24 78 0.15 79 0.23 80 0.71 81 6.09 82 0.15 83 0.19 84 0.11 85 0.1686 0.83 87 0.37

TABLE 28 Ex. IC₅₀ (μM) or inhibitory activity No. (%) at 30 μM in vitro88 0.16 89 0.12 90 0.29 91 1.53 92 0.69 93 0.51 94 0.11 95 0.12 96 0.2997 0.13 98 1.13 99 0.87 100 0.82 101 0.37 102 0.51 103 0.18 104 0.19 1050.10 106 0.23 107 0.65 108 0.16 109 0.17 110 0.15 111 1.10 112 3.09 1130.56 114 1.20 115 1.80

TABLE 29 Ex. IC₅₀ (μM) or inhibitory activity No. (%) at 30 μM in vitro116 0.18 117 0.39 118 0.64 119 0.64 120 0.12 121 0.33 122 0.96

Experimental Example 2 Human EPO Production Activity

The activity of the test compound on human EPO production was measuredusing Hep3B (AMC) established from human liver-derived cell line.

Hep3B cells were cultured in Eagle-MEM medium containing 10% fetalbovine serum, and the test compound was diluted with dimethyl sulfoxide(DMSO).

Hep3B cells were cultured in a 96-well plate, and a test compound wasadded at each concentration 24 hr later. After incubation at 37° C. for24 hr, the culture supernatant was collected. The concentration of humanEPO produced in the culture supernatant was measured using a humanEPO-ELISA kit (manufactured by StemCell Technologies, 01630) accordingto the manufacturer's explanation, and the human EPO production activity(%) of the test compound was calculated based on the maximum value ofproduction under the above conditions and the value without addition ofthe test compound. The human EPO production activity of each compound isshown by EC₅₀ (μM) or as human EPO production activity (%) at 30 μM inthe following Tables 30 to 34. In these Tables, the values consistingsolely of numbers show EC₅₀ (μM) and those containing % show human EPOproduction activity (%) at 30 μm.

TABLE 30 Ex. EC₅₀ (μM) or production activity No. (%) at 30 μM in vitro1 9.9 2 10.9 3 12.4 4 38%  5 11.5 6 20.8 7 18.4 8 13.4 9 1% 10 0% 11 1%12 5% 13 1% 14 5.1 15 29.1 16 7.0 17 8.8 18 6.1 19 6.6 20 6.6 21 12.0 2213.7 23 7.8 24 5.4 25 14.1 26 7.5 27 7.7 28 13.9 29 11.3

TABLE 31 Ex. EC₅₀ (μM) or production activity No. (%) at 30 μM in vitro30 15.4 31 12.1 32 15.6 33 10.1 34 15.0 35 43% 36 10.5 37 11% 38 8.7 3922.3 40 17.7 41 9.1 42 14.2 43 23.6 44 10.4 45 9.9 46 4.8 47 12.0 48 4.549 11.7 50 5.6 51 9.1 52 10.4 53 8.9 54 4.5 55 8.9 56 8.4 57 4.7 58 4.7

TABLE 32 Ex. EC₅₀ (μM) or production activity No. (%) at 30 μM in vitro59 49% 60 8.4 61 28.8 62 10.1 63 19.7 64  0% 65 49% 66 21.1 67 14.3 68 0% 69 12.0 70  1% 71 15.8 72 4.0 73 34% 74 8.3 75 23.7 76 18.0 77 18.778 6.6 79 7.8 80 23.3 81 33% 82 5.4 83 20.7 84 11.0 85 20.6 86  6% 8718.5

TABLE 33 Ex. EC₅₀ (μM) or production activity No. (%) at 30 μM in vitro88 14%  89 4.2 90 16.6 91 43%  92 18.5 93 16.0 94 9.7 95 4.3 96 5.9 973.5 98 25.6 99 20.2 100 18.0 101 6% 102 16.0 103 6.9 104 6.3 105 5.9 1066.0 107 4% 108 8.9 109 13.7 110 6.5 111 0% 112 0% 113 0% 114 0% 115 0%

TABLE 34 EC₅₀ (μM) or production Ex. No. activity (%) at 30 μM in vitro116 5.6 117 7.7

As is clear from the above-mentioned results, the compound of thepresent invention or a pharmaceutically acceptable salt thereof, or asolvate thereof has a human PHD inhibitory activity and a human EPOproduction activity.

INDUSTRIAL APPLICABILITY

The compound of the present invention or a pharmaceutically acceptablesalt thereof, or a solvate thereof inhibits binding of HIF and PHD basedon its PHD inhibitory activity and stabilizes HIF, which enablespromotion of EPO production.

Hence, the compound of the present invention or a pharmaceuticallyacceptable salt thereof, or a solvate thereof can be a medicamenteffective for the prophylaxis or treatment of various diseases andpathologies (disorders) caused by decreased production of EPO, and canbe effectively used for the treatment of anemia.

1. A compound represented by the following formula [I], or apharmaceutically acceptable salt thereof, or a solvate thereof:

wherein the partial structural formula:

is a group represented by any of the following formulas:

R¹ is (1) a hydrogen atom, (2) a C₁₋₆ alkyl group, (3) a C₆₋₁₄ arylgroup, (4) a C₃₋₈ cycloalkyl group, (5) a C₆₋₁₄ aryl-C₁₋₆ alkyl group,or (6) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group; R² is (1) a hydrogen atom,(2) a C₁₋₁₀ alkyl group, (3) a C₆₋₁₄ aryl group optionally substitutedby the same or different 1 to 5 substituents selected from the followinggroup B, (4) a C₃₋₈ cycloalkyl group optionally substituted by the sameor different 1 to 5 substituents selected from the following group B,(5) a C₃₋₈ cycloalkenyl group optionally substituted by the same ordifferent 1 to 5 substituents selected from the following group B, (6) aheteroaryl group optionally substituted by the same or different 1 to 5substituents selected from the following group B (wherein the heteroarylhas, besides carbon atom, 1 to 6 hetero atoms selected from nitrogenatom, oxygen atom and sulfur atom), (7) a C₆₋₁₄ aryl-C₁₋₆ alkyl group(wherein C₆₋₁₄ aryl is optionally substituted by the same or different 1to 5 substituents selected from the following group B), or (8) a C₃₋₈cycloalkyl-C₁₋₆ alkyl group (wherein C₃₋₈ cycloalkyl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe following group B); R³ is (1) a hydrogen atom, (2) a halogen atom,(3) a C₁₋₆ alkyl group, (4) a C₆₋₁₄ aryl group, (5) a C₃₋₈ cycloalkylgroup, or (6) a C₆₋₁₄ aryl-C₁₋₆ alkyl group; and R⁴ and R⁵ are eachindependently (1) a hydrogen atom, or (2) a C₁₋₆ alkyl group, group B:(a) a halogen atom, (b) a C₁₋₆ alkyl group, (c) a C₃₋₈ cycloalkyl group,(d) a cyano group, and (e) a halo-C₁₋₆ alkyl group.
 2. The compoundaccording to claim 1 wherein the partial structural formula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof. 3.The compound according to claim 1, wherein the partial structuralformula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof. 4.The compound according to claim 1, wherein the partial structuralformula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof. 5.The compound according to claim 1, wherein the partial structuralformula:

is a group represented by the following formula

or a pharmaceutically acceptable salt thereof, or a solvate thereof. 6.The compound according to claim 1, wherein both R⁴ and R⁵ are hydrogenatoms, or a pharmaceutically acceptable salt thereof, or a solvatethereof.
 7. The compound according to claim 1, wherein R³ is a hydrogenatom, or a pharmaceutically acceptable salt thereof, or a solvatethereof.
 8. The compound according to claim 1, wherein R¹ is a hydrogenatom, or a pharmaceutically acceptable salt thereof, or a solvatethereof.
 9. The compound according to claim 1, wherein R² is (1) a C₁₋₁₀alkyl group, (2) a C₆₋₁₄ aryl group optionally substituted by the sameor different 1 to 5 substituents selected from the above-mentioned groupB, (3) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (wherein C₆₋₁₄ aryl is optionallysubstituted by the same or different 1 to 5 substituents selected fromthe above-mentioned group B), or (4) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group(wherein C₃₋₈ cycloalkyl is optionally substituted by the same ordifferent 1 to 5 substituents selected from the above-mentioned groupB), or a pharmaceutically acceptable salt thereof, or a solvate thereof.10. The compound according to claim 2, wherein both R⁴ and R⁵ arehydrogen atoms, or a pharmaceutically acceptable salt thereof, or asolvate thereof.
 11. The compound according to claim 10, wherein R³ is ahydrogen atom, or a pharmaceutically acceptable salt thereof, or asolvate thereof.
 12. The compound according to claim 11, wherein R¹ is ahydrogen atom, or a pharmaceutically acceptable salt thereof, or asolvate thereof.
 13. The compound according to claim 12, wherein R² is(1) a C₁₋₁₀ alkyl group, or (2) a C₆₋₁₄ aryl-C₁₋₆ alkyl group (whereinC₆₋₁₄ aryl is optionally substituted by the same or different 1 to 5substituents selected from the above-mentioned group B), or apharmaceutically acceptable salt thereof, or a solvate thereof.
 14. Acompound represented by the following formula [I-1] or apharmaceutically acceptable salt thereof, or a solvate thereof:

wherein the partial structural formula:

is a group represented by:

R¹¹ is (1) a hydrogen atom, (2) a C₁₋₆ alkyl group, (3) a phenyl group,(4) a C₃₋₈ cycloalkyl group, (5) a phenyl-C₁₋₆ alkyl group, or (6) aC₃₋₈ cycloalkyl-C₁₋₆ alkyl group; R²¹ is (1) a hydrogen atom, (2) aC₁₋₁₀ alkyl group, (3) a phenyl group optionally substituted by the sameor different 1 to 5 substituents selected from the following group B,(4) a C₃₋₈ cycloalkyl group, (5) a C₃₋₈ cycloalkenyl group, (6) athienyl group optionally substituted by the same or different 1 to 5substituents selected from the following group B, (7) a phenyl-C₁₋₆alkyl group (wherein phenyl is optionally substituted by the same ordifferent 1 to 5 substituents selected from the following group B), or(8) a C₃₋₈ cycloalkyl-C₁₋₆ alkyl group; R³¹ is (1) a hydrogen atom, (2)a halogen atom, (3) a C₁₋₆ alkyl group, (4) a phenyl group, (5) a C₃₋₈cycloalkyl group, or (6) a phenyl-C₁₋₆ alkyl group; and R⁴¹ and R⁵¹ areeach independently (1) a hydrogen atom, or (2) a C₁₋₆ alkyl group groupB: (a) a halogen atom, (b) a C₁₋₆ alkyl group, (c) a C₃₋₈ cycloalkylgroup, (d) a cyano group, and (e) a halo-C₁₋₆ alkyl group. 15.-25.(canceled)
 26. A pharmaceutical composition comprising the compoundaccording to claim 1, or a pharmaceutically acceptable salt thereof, ora solvate thereof, and a pharmaceutically acceptable carrier. 27.-34.(canceled)
 35. A method of inhibiting prolyl hydroxylase, comprisingadministering an effective amount of the compound according to claim 1,or a pharmaceutically acceptable salt thereof, or a solvate thereof to amammal.
 36. A method of inducing erythropoietin production, comprisingadministering an effective amount of the compound according to claim 1,or a pharmaceutically acceptable salt thereof, or a solvate thereof to amammal.
 37. A method of treating anemia, comprising administering aneffective amount of the compound according to claim 1, or apharmaceutically acceptable salt thereof, or a solvate thereof to amammal.
 38. A method of treating renal anemia, comprising administeringan effective amount of the compound according to claim 1, or apharmaceutically acceptable salt thereof, or a solvate thereof to amammal.
 39. A commercial package comprising the pharmaceuticalcomposition according to claim 26 and a written matter associatedtherewith, the written matter stating that the pharmaceuticalcomposition can or should be used for the treatment or prophylaxis of adisease selected from anemia and renal anemia.
 40. A kit comprising thepharmaceutical composition according to claim 26 and a written matterassociated therewith, the written matter stating that the pharmaceuticalcomposition can or should be used for the treatment or prophylaxis of adisease selected from anemia and renal anemia.